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International Virtual Conference on Plant Science and Agriculture Research
Dec 2024
World Congress on COPD and Pulmonary Diseases
Dec 2024
The Medical Device Summer School - From Concept to CE Marking
Dec 2024
Chromatography Fundamentals for Biologics Process Development
Dec 2024
A Regulatory Update on Animal Feed and Feed Additives in the EU, USA and China
Dec 2024
Global Webinar on Virology & Covid 19
Nov 2024
Hippo Pathway Targeted Drug Development Summit
Nov 2024
Antibody Engineering with Novel Technologies Online Symposium
Nov 2024
Case Reports
Nov 2024
Glycobiology
Nov 2024
Drafting and Negotiating Clinical Trial Agreements
Nov 2024
The International Electronic Conference on Foods The Future of Technology, Sustainability, and Nutrition in the Food Domain
Oct 2024
The International Electronic Conference on Brain Sciences
Oct 2024
Advanced Screening Approaches in Drug Delivery
Oct 2024
Indegene Digital Summit Virtual
Oct 2024
The International Online Conference on Bioengineering (IOCBE)
Oct 2024
The International Electronic Conference on Diversity (IECD)
Oct 2024
International Conference on Advances in Biological Science and Technology (ICABST)
Sep 2024
Oligo Chemistry and Therapeutics Online Symposium
Sep 2024
Cell Culture & Quality Control Online Symposium
Sep 2024
International Conference on Bioscience & Engineering (BIOSE)
Sep 2024
Oncological Advancements Online Conference
Sep 2024
Plants & Agro Online Conference
Sep 2024
Electrophysiology Review for Boards and Recertification
Sep 2024
Cell Bank Establishment & Testing MasterClass - EU
Sep 2024
Strategic Staffing in Life Sciences
Jul 2024
International Forum on Biotechnology and Genetic Engineering (BIOTECHFORUM)
Jul 2024
Microbiological Contamination Control MasterClass - US
Jul 2024
International Conference on Biology and Life Sciences (ICBLS)
Jun 2024
International Electronic Conference on Processes - Green and Sustainable Process Engineering and Process Systems Engineering (ECP)
May 2024
Indian Scientist Meet
May 2024
Life Science Technical Accounting CPE Update
May 2024
International Conference on Biomedicine (ICBM
May 2024
Advanced Protein Aggregation & Characterization
Apr 2024
International Conference on Life Sciences (LiSci)
Apr 2024
International Conference on Advanced Nanoscience and Technology (ANaNO)
Apr 2024
International conference on Bioinformatics and computational studies (ICBCS)
Apr 2024
Global Meet on Biotechnology and Bioscience (GMBB)
Mar 2024
Toxicology, ADME & Early Drug Development Plan
Mar 2024
International Conference on Clinical Pharmacy and Pharmaceutical Research (ICCPPR)
Dec 2023
Edition of International Conference on Microbiology, Antibiotics and Public Health
Dec 2023
BMSeCON - International e-Conference
Dec 2023
International Conference on Immunology Infectious Diseases
Nov 2023
The International Electronic Conference on Agriculture
Nov 2023
Global Summit and Expo on Biotechnology and Bioscience (GSEBB)
Oct 2023
Pediatric Early Development Symposium (PEDS)
Oct 2023
International Conference and Exhibition on Natural Products Chemistry and Medicinal Plants Research
Oct 2023
International Conference on Agricultural and Food Science ( ICAFS)
Oct 2023
Antibodies, Next-Generation Proteins Therapeutics Summit
Sep 2023
The International Electronic Conference on Toxins
Jul 2023
CFR Part 11 Guidance for Electronic Records and Electronic Signatures in FDA-Regulated Industries
Jun 2023
ISMOS - The International Symposium on Applied Microbiology and Molecular Biology in Oil Systems
Jun 2023
Biodetection Technologies
Jun 2023
Stability & Shelf Life of Biologics
May 2023
Comparability for Biologics
Apr 2023
Antibody Engineering & Therapeutics ASIA
Apr 2023
Bioassays & Bioanalytical Methods
Apr 2023
Global Summit on Physiology and Metabolism of Thyroid
Apr 2023
Pediatrics & Neonatology Conference
Apr 2023
International Conference on Bioinformatics and Computational Biology (BICOB)
Mar 2023
Designing Molecular Glues
Mar 2023
International Conference on Global issues in Multidisciplinary Academic Research
Mar 2023
Life Sciences, Clinical Trials, Patient Recruitment & Retention
Jan 2023
Strategy for Cell & Gene Therapies
Jan 2023
Life Sciences, Commercialization & HEOR - 4 Key Trends for Commercial Success in
Jan 2023
International Conference on Sustainable Development
Dec 2022
Evaluating Biopharma - Cell Therapy Strategies
Dec 2022
World Congress on Animal Science and Veterinary Medicine
Dec 2022
Project Management for Pharma Professionals
Dec 2022
TIGIT Therapies Digital Summit
Dec 2022
World Congress on Clinical Microbiology and Infectious Diseases
Dec 2022
FAAM-EUROBAT Digital
Dec 2022
International Conference on Drug Discovery and Drug Development
Nov 2022
Technical Documentation to Comply with the MDR (Medical Device Regulation) and IVDR (In-Vitro Diagnostic Regulation)
Nov 2022
Global Summit On Medicinal Plants And Natural Products
Oct 2022
International Conference on Nanomedicine and Drug delivery
Sep 2022
International Summit on Genomics and Proteomics
Sep 2022
International Conference on Cell & Stem Cell Research
Sep 2022
World Forum for Women in Science
Sep 2022
Multinational Congress on Microscopy
Aug 2022
International Conference On Pharmacology And Toxicology
Aug 2022
Analytical Instrument Qualification & Validation - Use of Excel and FDA Audit Preparation
Jul 2022
European Conference on Rare Diseases and Orphan Products (ECRD)
Jul 2022
Congress on Polycystic Ovarian Syndrome and Fertility
Jun 2022
International conference on Clinical Nutrition and Fitness
Jun 2022
Global conference on neuroscience and Psychiatry
May 2022
International Conference on Cancer Stem Cells and Oncology Research
May 2022
Due Diligence for Life Sciences Summit
May 2022
Conference on Parasitology & Infectious Diseases
May 2022
Global Summit on Cancer And Oncology Research
May 2022
U.S. FDA and EU Medical Device Directive Requirements for DHFs, DMRs, DHRs, and TF/DDs
May 2022
International Conference on Drug Discovery & Toxicology
May 2022
Pharmacokinetics (PK) / Pharmacodynamics (PD) Studies in Drug Discovery and Development
May 2022
AICR Lifestyle and Cancer Symposium - Innovation to Impact
Apr 2022
Nasal Drug Delivery
Apr 2022
International Conference and Exhibition on Nanomedicine and Pharmaceutical Nanotechnology
Apr 2022
International Conference on Biomaterials, Cellular and Tissue Engineering
Apr 2022
International Conference on Hematology and Bone Marrow Transplantation
Apr 2022
International Conference on Molecular Medicine and Diagnostics
Apr 2022
International Conference on Clinical Research and Clinical Trials
Mar 2022
Animal Science and Veterinary Medicine
Mar 2022
Middle East Veterinary Medicine & Animal Science Conference (MEVMAS)
Feb 2022
Quality Control Laboratory Compliance - cGMPs and GLPs
Feb 2022
3D Cell Culture
Feb 2022
International Conference on Bacteriology and Infectious Diseases
Dec 2021
International Conference on Toxicogenomics
Dec 2021
Stem Cell-based Modelling of Development and Disease
Dec 2021
World Congress on Cell and Structural Biology
Dec 2021
International Viral Hepatitis Elimination Meeting (IVHEM)
Dec 2021
International Conference on Microbiology and Infectious diseases
Nov 2021
Global Conference on Cleaning Validation
Nov 2021
Biotherapeutics US
Nov 2021
Wnt & B-Catenin Targeted Drug Discovery Summit
Nov 2021
WSAVA Global Community Congress
Nov 2021
dLaw Life Sciences Summit
Nov 2021
The International Conference on Biodiversity and Environmental Management (BEM)
Nov 2021
Vendor/CRO Management and Oversight MasterClass
Nov 2021
International Scientific Conference on Probiotics, Prebiotics, Gut Microbiota and Health (IPC)
Oct 2021
International Partnering Conference (BIO-Europe)
Oct 2021
EU Pharmaceutical Regulations & Strategy
Oct 2021
ASHG - American Society of Human Genetics Meeting
Oct 2021
International Conference on Computational Systems-Biology and Bioinformatics (CSBio)
Oct 2021
International Conference on Plant Tissue Culture & Genetics
Oct 2021
Leaders in Biobanking Congress
Oct 2021
NHLBI Progenitor Cell Translational Consortium (PCTC)
Sep 2021
Temperature Control and Logistics US
Sep 2021
World Climate Change Congress
Sep 2021
International Conference on Engineering, Science, Technology & Management (ICESTM)
Sep 2021
MedTech & Diagnostics Value & Access USA
Sep 2021
International Conference on Plant and Molecular Biology (PMB) webinar
Aug 2021
International Conference on Research in Life-Sciences & Healthcare (ICRLSH)
Aug 2021
Microscopy & Microanalysis (M&M)
Aug 2021
Congress on Environmental Pollution and Health
Aug 2021
Congress on Clinical Microbiology and Yeast Congress
Jul 2021
International Conference on Digestive and Metabolic Diseases
Jul 2021
Congress of European Microbiologists (FEMS)
Jul 2021
Global Bioprocessing: Pharma 4.0 Summit
Jun 2021
Biologics Formulation Development and Drug Delivery Forum
Jun 2021
Society of Nuclear Medicine and Molecular Imaging (SNMMI) Annual Meeting
Jun 2021
Employment Law in Practice from Recruitment to Termination
May 2021
International Conference on Medical and Clinical Microbiology
May 2021
Conference on Plant Genomics, Horticulture and Engineering
May 2021
SMi`s Pain Therapeutics Conference
May 2021
Experimental Biology (EB)
Apr 2021
Biologics Europe Online
Apr 2021
Clinical Trials V-Forum
Apr 2021
Tumor & Cancer Immunology and Paediatric-Oncology
Apr 2021
Latin America - Understanding Regulatory Compliance Requirements Across the Life Science Industry (Focus: Brazil, Mexico, Argentina)
Apr 2021
Virtual On-line Conference on Clinical Trials & Clinical Research
Mar 2021
Biotherapeutics Analytical Summit
Mar 2021
Ensuring Compliance with Advertising and Promotional Requirements for Drugs and Medical Devices
Mar 2021
New Medical Device Regulation
Mar 2021
World Congress on Clinical Microbiology and Infectious Diseases
Mar 2021
Supply Chain Re-Innovation: Life Sciences
Mar 2021
The Plant Genomics and Gene Editing Congress Europe
Mar 2021
Risk Management in Medical Devices Industry
Mar 2021
Medical Writing for Medical Devices
Mar 2021
Medical Writing Landscape Advancement Summit
Mar 2021
Patentability and State of the Art Searching
Feb 2021
Molecular Med TRI-CON
Feb 2021
ICMIB: International Conference on Medical Information and Bioengineering
Feb 2021
FDA`s Medical Device Software Regulation Strategy
Feb 2021
MedAffairs for MedTech & Diagnostics
Feb 2021
Change Control Best Practices - Avoiding Unintended Consequences of Changes
Jan 2021
EC Medical Devices Vigilance System and Post Marketing Surveillance
Jan 2021
Data Integrity: FDA/EU Requirements and Implementation
Jan 2021
PepTalk: The Protein Science Week
Jan 2021
International Conference on Virology & Novel Coronavirus Diseases
Dec 2020
World Biomaterials Congress (WBC Virtual)
Dec 2020
World Summit on Allergy and Clinical Immunology
Dec 2020
International Fluid Academy Day (IFAD)
Nov 2020
Impact of the Covid-19 Pandemic on Cancer patients
Nov 2020
Product Launch Excellence for Pharma & Biotech
Nov 2020
Business Development and Licensing in Pharma and Biotech
Nov 2020
Proteome - Targeted Drug Discovery Summit
Nov 2020
Brazil School for Single Particle Cryo-EM
Nov 2020
Plant Biology Virtual
Nov 2020
Essentials Of USP Microbiology - For Those Who Are Not Microbiologists or Who Wish A Refresher
Oct 2020
Global Experts Meet on Biotechnology and Biomedical Engineering
Oct 2020
Global Experts Meet on Genetics and Genomics
Oct 2020
FDA`s Regulation of Regenerative Medicine including Stem Cell Treatments and Tissue Engineering Training
Oct 2020
Global Experts Meeting on Parkinson`s & Movement Disorders
Oct 2020
International Conference and Expo on Pharmacognosy, Medicinal Plants and Natural Products
Oct 2020
nanomedicine-pharma
Oct 2020
Annual Congress on Immunology & Immunogenetics
Oct 2020
B-Cell Directed Therapies for Autoimmune Diseases
Oct 2020
International Conference on Animal Science and Animal Health Management
Oct 2020
Global Conference on Stem Cell & Regenerative Medicine
Oct 2020
Project Management for FDA-Regulated Companies
Oct 2020
Glycobiology, Lipids and Metabolic Disorders
Oct 2020
International Cancer Study & Therapy Conference
Oct 2020
World Congress on Biosensors and Bioelectronics
Sep 2020
International Conference on Enzymology and Protein Chemistry
Sep 2020
Risk Management in Clinical Research
Sep 2020
EuroSciCon Conference on Biotechnology & Bioengineering
Sep 2020
Global Summit on Plant Science
Sep 2020
Digital Edible Insects Innovation Summit
Sep 2020
Virtual Conference on Future of Science (SciCon)
Sep 2020
International Conference on Nucleic Acids
Sep 2020
International conference on Neurology and Neuroscience
Sep 2020
International Conference on Neuroscience and Neurochemistry
Sep 2020
EFMC International Symposium on Medicinal Chemistry (EFMC-ISMC)
Sep 2020
International Conference on Science & Technology Research (ICSTR London)
Sep 2020
Life Science Regulatory Information Summit
Aug 2020
International Conference on Pharmacology and Pharmaceutical Medicine (ICPPM)
Aug 2020
Medicinal Development of Cannabis and Cannabinoids
Aug 2020
Euro Biosensors and Bioelectronics Conference
Aug 2020
Congress on Neuroscience and Therapeutics
Jul 2020
International Virtual Conference on Agriculture and Aquaculture
Jul 2020
International Conference on Cell and Stem Cell Research
Jul 2020
Validation, Verification and Transfer of Analytical Methods (Understanding and implementing guidelines from FDA/EMA, USP and ICH)
Jul 2020
International Conference and Expo on Proteomics and Bioinformatics
Jul 2020
International Webinar on Plant Science and Molecular Biology
Jul 2020
International Conference on Pharmacology and Nanotechnology
Jul 2020
Biomanufacturing Congress
Jul 2020
Nanomedicine and Nanobiotechnology (iNanomedince)
Jun 2020
World Congress on Microbiology and Rare Infectious Diseases
Jun 2020
International Conference on Cell and Gene Therapy
Jun 2020
TechXchange: Healthcare & Life Sciences
Jun 2020
Annual Congress on Pharmaceutics & Drug Delivery Systems
Jun 2020
Cancer and Metabolism
Jun 2020
Bio International Convention (BIO)
Jun 2020
International Conference on Structural Biology
Jun 2020
Market Access Latin America Leaders Forum
Jun 2020
International Conference on Integrative Biology
Jun 2020
LifeScience Micro MBA MasterClass
May 2020
Congress on Plant Science and Molecular Biology
May 2020
International Conference on Neurological Disorders and Stroke
May 2020
Sea Foods & Aquaculture
May 2020
SMi`s Superbugs and Superdrugs Conference
Mar 2020
You have a BI Positive or Product Sterility Positive - Now What
Nov 2019
CDISC Mapping 5: ADAM Models - ADSL, BDS and ADAE
Sep 2019
How to Investigate Environmental Monitoring Excursions
Sep 2019
Process Validation - Overview of Why and How
Jul 2019
Quality Control for Microbiological Media and Reagents
Jun 2019
Latin America – Understanding Regulatory Compliance Requirements Across the Life Science Industry
May 2019
Quality Control for Microbiological Media and Reagents
May 2019
GMP Environmental Monitoring in Pharmaceutical Clean Rooms
May 2019
ISO 14971:2012 - Does your current Risk Analysis still comply with your CE Mark requirements
Apr 2019
QbD Approach to Analytical Method Lifecycle: Design, Development, Validation and Transfer
Mar 2019
The Most Serious FDA 483s - How to Avoid Them
Mar 2019
Water System Biofilm Control and Microbial Monitoring Myths
Mar 2019
Measurement Uncertainty in Microbiology
Mar 2019
Is it Method Verification or Validation, or Just Semantics
Feb 2019
GDPR and Implications on Drug Development
Feb 2019
An Advanced Course on Lean Documents, Lean Configuration and Document Control
Feb 2019
Validation and Use of Excel Spreadsheets in FDA Regulated Environments
Feb 2019
Controlled Document System for a Life Sciences Manufacturing Plant - Principles of Lean Documents and Lean Configuration
Jan 2019
Water System Mythology: Common False Beliefs for Microbial Control and Monitoring
Jan 2019
Verification vs. Validation in Regulated Industries
Jan 2019
Particulates in Biological Products - Evolving Regulations for Testing in Clinical and Commercial Stages
Dec 2018
Meet the Tougher U.S. FDA CGMPs
Nov 2018
Troubleshooting Ethylene Oxide (EO) Processes
Oct 2018
Powerful Closed-loop CAPA - Meeting FDA Expectations
Oct 2018
Advancing Pathology for Cancer Diagnosis, Staging and Prognosis
Aug 2018
Building a Compliant Documentation and Training System
Aug 2018
Opioid Abuse in the Workplace: Using Effective Drug Testing and Policies to Reduce the Pain of the Painkiller Epidemic
Jul 2018
Sunshine Act Reporting: Clarification for Clinical Research
Jul 2018
Onboarding In A GMP Environment – Best Practices
Jul 2018
Japan - Regulatory Filing Requirements and Compliance Processes for Life Sciences
Jul 2018
Develop a Compliant Validation Protocol and Analytical Procedures according to the FDA Guidance and USP Good Documentation Practices
Jul 2018
Current Regulatory Requirements for Sterile Products
May 2018
How to Achieve a Compliant and Effective Cleanroom Design and Facility Validation
May 2018
Document Control and Change Control Process in GxP/GMP Environment
May 2018
Health Product Marketing authorization in Brazil - Documentation, Approval Process, Labeling, Advertising and Post Market Vigilance
May 2018
Analytical Method Validation
Mar 2018
FDA Clinical Trial Auditing and the due diligence Companies should conduct as part of their monitoring program
Mar 2018
Analytical Method Validation Under Good Laboratory Practices - GLPs
Dec 2017
Best Practices for an Effective Cleaning Validation Procedures
Sep 2017
Advances in Cellular Therapy
Sep 2017
Understanding Aseptic Technique and Cleanroom Behavior
Jul 2017
How To Establish an Effective Chief Compliance Officer`s (CCO) or Chief Risk Officer`s (CRO) Function - Organization and Responsibilities
Jun 2017
Advancing Alzheimer`s Research: Characterisation, Diagnosis & Treatment
Jun 2017
HIPAA and Human Resources
Jun 2017
How to Manage the HIPAA Business Associate Process
Jun 2017
Elements of a Corrective and Preventive Action (CAPA) Program and Uses of CAPA Data
May 2017
Lessons Learned in the Design, Installation, Start-Up and Qualification of Clean Compressed Air Systems for cGMP Manufacturing
Apr 2017
TM’s World Molecular & Cell Biology Online Conference
Apr 2017
The Obesity Epidemic: Discussing The Global Health Crisis
Apr 2017
Introduction to Design of Experiments
Apr 2017
What You Should Know About Export Requirements for FDA Regulated Products from the US to Foreign Countries
Apr 2017
Verification or Validation of Methods in Food Microbiology
Mar 2017
21 CFR Part 820 Quality System Regulation - Applying Principles of Lean Documents and Lean Configuration
Mar 2017
Compliance Trainings ASQ Certified Quality Engineer (CQE) Exam Preparatory Course
Mar 2017
The Forensic Forums
Mar 2017
21 CFR Part 820 - Quality System Regulation - Applying Principles of Lean Documents and Lean Configuration
Feb 2017
Trial Master File (TMF): FDA Expectations from Sponsors and Sites
Feb 2017
Ageing
Feb 2017
Three-dimensional cell culture: Innovations in tissue scaffolds and biomimetic systems
Feb 2017
Spotlight on Post Market Surveillance
Feb 2017
The Sports Science Summit
Jan 2017
Bacteriophage
Jan 2017
Transfer of Analytical Methods and Procedures: FDA Requirements and Strategies and Tools for Implementation
Dec 2016
Reinventing Remote Monitoring to Improve Clinical Trial Quality
Dec 2016
Improving techniques and technology for cellular and molecular pathology
Dec 2016
Innate Immunity: The line of defence
Nov 2016
Developing antibiotic alternatives: A discussion of new approaches to overcoming antimicrobial resistance
Nov 2016
Vaccine Antigen Delivery: new approaches to vaccine development
Oct 2016
Laboratory Investigation Out-of-Specification Results
Oct 2016
Design and Execution of Stability Studies for Biologics
Oct 2016
Acceptance Activities in FDA QSR
Oct 2016
Lyophilization: What you Need to Know, Validation and Regulatory Approaches
Oct 2016
HIPAA Training for the Compliance Officer
Oct 2016
Biopharmaceuticals as Therapeutic Agents Product and Process Development and Evaluation
Sep 2016
Sub-visible Particulates in Biological products
Sep 2016
Pregnancy and Childbirth
Sep 2016
Moving Forward with Stem Cell Therapy
Sep 2016
TM’s World Neurology Online Conference
Sep 2016
Lyophilization: What you Need to Know, Validation and Regulatory Approaches
Aug 2016
Interpreting and Reporting Descriptive Statistics
Aug 2016
FDA Issues Draft Guidance for 3D Printed Medical Devices
Jul 2016
Good Documentation Practices (GDP)
Jul 2016
Labeling of genetically modified organisms (GMO`s) in the USA
Jun 2016
21 CFR 111 GMP Dietary Supplement Laboratory
Jun 2016
Analytical Method Validation under Good Laboratory Practices (GLPs)
Jun 2016
Adverse Event Reporting: Site and Sponsor Reporting Requirements for Investigational Products
May 2016
Implementing Validation and Qualification - Annex 15 and FDA Requirements
May 2016
Blood Borne Pathogens
Apr 2016
Mathematics of Terminal Sterilization - Probability of Survival Approach -vs- Overkill Approach
Mar 2016
Sterile Filtration of Pharmaceutical Products - What you need to know to meet Validation and Regulatory Requirements - By AtoZ Compliance
Mar 2016
Sterilization Processes: The Methods, Parameters and Deficiencies Often Cited
Feb 2016
Payroll Technology
Jan 2016
How to Develop a strong CAPA System by Understanding its Unique Challenges
Jan 2016
Investigational Device Accountability
Jan 2016
Effective Design Controls in Accordance with Subpart C of 21 CFR, Part 820
Jan 2016
Established Condition - The New FDA Guidance
Jan 2016
Drug Master Files: New Implications under GDUFA
Jan 2016
U.S. FDA`s Strategic Priorities - and Beyond
Jan 2016
Design Inputs - Design Outputs Traceability Matrix - Principles of Lean Documents and Lean Configuration
Jan 2016
Statistical Process Control
Jan 2016
FDA Inspections : Managing the Myth and the Reality
Jan 2016
Risk Management and Risk-Based Monitoring
Jan 2016
Creating and Maintaining a GMP Quality System
Jan 2016
Process Robustness: The New FDA Paradigm
Jan 2016
How to Detect Lack of Data Integrity
Jan 2016
FDA`s New Enforcement of 21 CFR Part 11
Jan 2016
Incorporating Risk Management into Process Improvement
Jan 2016
FDA Compliance and GAMP V Computer System Classification
Jan 2016
Writing Effective Standard Operating Procedure (SOPs)
Jan 2016
The Federal False Claims Act: Becoming a Whistleblower
Dec 2015
Complaint Handling Requirements - Interrelationship with CAPA, Change Control, Adverse Event Reporting and Recalls, Life Cycle Process Activities
Dec 2015
HIPAA - Portable Devices and Enforcement
Dec 2015
Safe Drinking Water - Another Oxymoron?
Dec 2015
Objectionable Microorganisms: Considering the Risk
Dec 2015
Building a Vendor Qualification Program for FDA Regulated Industries
Nov 2015
An Easy to Implement Integrated Risk Management Approach Compliant with ISO 14971
Oct 2015
Product Stability Testing Program - Designing and Sustaining New and Existing Programs
Oct 2015
How to Survive a DEA Inspection Series: Controlled Substances and Hospital Pharmacy
Oct 2015
Is your Essential Requirements Checklist (ERC) up to snuff?
Oct 2015
Risk Management in Clinical Trials
Oct 2015
Extending Drug`s Life
Oct 2015
Establishing an FDA-Compliant UDI System
Oct 2015
How to Buy COTS Software, and Audit and Validate Vendors
Oct 2015
An Easy to Implement Integrated Risk Management Approach Compliant with ISO 14971
Sep 2015
Budgeting for Clinical Trials: Understanding Costs of a Study and Which Costs Sponsors are Responsible to Cover
Sep 2015
Application of Lean Six Sigma Methodology for Regulated Industries
Sep 2015
How to Transition from Paper to Electronic Records in a Regulatory Environment
Sep 2015
Laboratory Accreditation: Getting there is Just the Beginning
Sep 2015
CAPA Investigations - Tools for a Compliant and Effective Investigation Process
Sep 2015
Getting to Know FDA Audit Practices and the 10 Most Common Cited GMP Deficiencies
Aug 2015
Key Considerations in Verification & Validation of Medical Devices
Aug 2015
Creating a Global Regulatory Plan
Aug 2015
Understanding FDA Regulations and Role in Opioid Pain Management
Aug 2015
Understanding the Mobile Medical Applications Guidance
Aug 2015
DHF, DMR, DHR, Technical File and Design Dossier - Key Requirements and Future Directions
Jul 2015
21 CFR Part 820 - Quality System Regulation - Applying Principles of Lean Documents and Configuration
Jul 2015
FDA Inspection and Medical Device Design Control
Jul 2015
USP Hot Topics: What`s Hot Now and How to Track Coming Changes and Influence USP
Jul 2015
Validation of Complex Cell-Based Potency Methods
Jul 2015
The Future of OTC Drug Regulation and the Monograph Process
Jul 2015
Navigating the New FDA Draft Guidance on ISO 10993: Biological Evaluation of Medical Devices
Jul 2015
Conducting Audits in Non-English Locales - How to Ensure that Best Practices are Followed
Jul 2015
Preparing for the LDT Regulation
Jul 2015
Uncertainty of Measurement as Required by ISO/IEC Standard 17025:2005 for Lab Accreditation:An Environmental Microbiologist’s Perspective
Jul 2015
Using Q-Submission to Most Effectively Prepare for an FDA 510(k) Submission
Jul 2015
Normality Tests and Normality Transformations
Jun 2015
South East Asia Regulatory Compliance for Life Science Products, Live Webinar
Jun 2015
A CAPA Primer - Elements of a CAPA Program
Jun 2015
How to Develop PAT Approach-Regulatory Compliance
Jun 2015
Conducting Observational Studies in US, Canada and Europe
Jun 2015
TM`s World Neuroscience Online Conference
Jun 2015
Supplier Quality Management - Implement it Now or Pay for it Later
Jun 2015
Monitoring Plans: 10 Rules of Effective Writing of Monitoring Plans
May 2015
The FDA Inspection: Preparation, Management, and Follow-Up
May 2015
Optimal Resource Allocation and Capacity Planning for Biopharma and CRO
May 2015
CAPA, Failure Investigation and Root Cause Analysis - FDA Expectations
May 2015
Ensuring Data Integrity for FDA/EU Compliance
May 2015
Writing Effective Journal Abstracts: A Guide for Medical Writers and Clinical Research Professionals
May 2015
Complaint Handling in Compliance with FDA and ISO Regulations
May 2015
Change Control - Key to Successful cGMP Compliance
Apr 2015
UDI Implementation
Apr 2015
Electronic Records and Signatures - 21 CFR Part 11: Basic Concepts
Apr 2015
Is it Method Verification or Validation, or Just Semantics?
Apr 2015
Combination Drug/Device Products CGMPs - Final Rule
Apr 2015
China: Compliance Processes for Life Science Products (Company Establishment, Clinical Trials, Registrations, Renewals and Supply Chain Considerations)
Apr 2015
Health Canada’s Enforcement of the Regulatory Requirements for the Manufacture, Advertising and Sale of Pharmaceuticals, Medical Devices and Natural Health Products
Mar 2015
Designing Effective and Efficient Extractables or Leachables Studies for Biologics
Mar 2015
Biological Facility Design for Compliance
Mar 2015
Biomedical Software Regulation
Mar 2015
New Part 11 Guidance for Clinical Trials: What This Means for You
Mar 2015
Avoid Warning Letters in View of the U.S. FDA`s Stated Goal
Mar 2015
Superiority, Non-inferiority, or Equivalence Trials: How, Why and When
Mar 2015
Epigenetic Editing - towards reprogramming of gene expression
Mar 2015
Metabolic regulation of cell death
Mar 2015
Institutional Review Boards (IRBs): The Changing Landscape and the Effect on the Conduct of Clinical Research
Mar 2015
How to Avoid an FDA Warning Letter with a Strong CAPA Program
Mar 2015
Complaint Handling and Management: From Receipt to Trending
Feb 2015
TM’s world cancer online conference
Feb 2015
DNA methylation changes during cell differentiation
Feb 2015
Auditing for Microbiological Aspects of Pharmaceutical and Biopharmaceutical Manufacturing
Feb 2015
Blinding of Investigational Materials
Feb 2015
The FDA 510(k) and Q-Submission: Best Practices
Feb 2015
Changing Supplier Controls Requirements
Feb 2015
Diagnostics & Biomarkers (DB)
Jan 2015
Understanding the pathways of necroptotic cell death, free webinar
Jan 2015
Benchmark for Cleaning Validation
Jan 2015
New Requirements for Sponsors and Laboratories for Analyzing Clinical Trial Samples to Meet GCP/GCLP Internationally
Jan 2015
What is the harm in that? Risk Management 101
Jan 2015
EU Clinical Trial Regulation: New Requirements
Jan 2015
21 CFR Part 11 and Annex 11 Compliance - specifics needed to eliminate 483s
Jan 2015
The FDA Drug Approval Process
Jan 2015
A step-by-step guide to ChIP-seq data analysis, free webinar
Dec 2014
What are Serious Adverse Events & How do I Handle SAEs?
Nov 2014
Applications of ChIP
Nov 2014
Advances in Stem Cell Research (ASCR2014)
Sep 2014
Current Good Manufacturing Practices (cGMP) for Medical Devices and IVDs
Sep 2014
Know your regulators: Pharmaceutical Regulatory Agencies and Organizations around the World: Scope and Challenges in Drug Development
Jul 2014
Preparing for an FDA API GMP Inspection
Jul 2014
Effective Contamination Control in Biopharmaceutical Manufacturing
Jul 2014
Developing Biosimilars in Emerging Markets: Regulatory and Clinical Considerations
Jul 2014
Drug Discovery & Development (DDD)
Jun 2014
TM`s World Genetics & Genomics Online Conference
May 2014
China: Compliance Processes for Life Science Products (Company Establishment, Clinical Trials, Registrations, Renewals and Supply Chain Considerations)
May 2014
Lighting Up the Pathways to Cell Death: Fluorescence Microscopy Approaches to Measuring Caspase Activation
Mar 2014
Epigenetic dynamics in stem cells and differentiation
Feb 2014
Clinical Trial Design for Personalised Medicine Webinar
Nov 2013
Remediating Pharmaceutical Water System Biofilm - What to Do After It Gets Ahead of You
Nov 2013
Social Media and Marketing FDA Regulated Products
Nov 2013
Robust Corrective And Preventive Action (CAPA)
Nov 2013
Annual Digital Marketing Strategies for Patient Outreach
Nov 2013
Corrective and Preventive Actions(CAPA) - 8 Steps to Achieve Compliance
Nov 2013
Principles and Practice of Confocal Microscopy in Life Sciences
Nov 2013
Principles and Practice of Confocal Microscopy
Nov 2013
Study to Support Shipping and Distributing Pharmaceutical Products
Oct 2013
Premarket Review of New and Modified Tobacco Products
Oct 2013
3-hr Virtual Seminar: US, EU and Japan GMP Requirements: Practical ICH Area Differences, Healthcare Authority Inspection Focus
Oct 2013
Water System Mythology: Common False Beliefs for Microbial Control and Monitoring
Oct 2013
FDA`s Oversight of Mobile Medical Applications (`apps`) for Use on Smartphones and Similar Mobile Devices
Sep 2013
Effective CAPAs: How to Avoid Scrutiny in FDA’s Latest Area of Focus
Sep 2013
FDA Requirements for Device Labeling: Development, Contents, Distribution, and Changes
Aug 2013
Coping with a Difficult Compliance Officer when Responding to a 483, Warning Letter, Import Alert or Recall
Aug 2013
Regulatory Differences Between Biopharmaceutics and Medical Devices
Aug 2013
CAPA – The Heart of Your Quality System
Jul 2013
FDA and Social Media - How to Promote your Products Using Web 2.0 in Compliance with FDA and FTC Laws and Regulations
Jun 2013
Introduction to Bioequivalence and Therapeutic Equivalence
Jun 2013
Shared facilities and the move to science based risk assessments
Jun 2013
Serious Product Quality Problems – Dealing with the Press and the Public
Jun 2013
Key Issues in FDA & FTC Regulation of Dietary Supplements
May 2013
FDA Warning Letter Closeout Program
May 2013
Complaint Systems – The Essential Requirements
May 2013
The US FDA Quality System Regulation (QSR) – What Every Exective and Senior Manager Must Know
May 2013
e-Submissions & Data Standards for FDA (eCTD, CDISC, HL7)
May 2013
Statistics for GMP Auditors
Apr 2013
How to Make GMP Training Fun and Engaging
Apr 2013
How to Withstand an FDA Audit of your Facility
Apr 2013
When is Corrective Action Not Enough - Doing and Documenting Corrections is an ISO 13485 Expectation
Apr 2013
3-hr Virtual Seminar: Annual ICH GCP Refresher Course
Apr 2013
Designing a Clinical Protocol for Vaccine Clinical Trial
Apr 2013
Microbiological Risk: Do I Really Need to Test Raw Materials for Microorganisms
Mar 2013
Writing Clinical Data Queries - Best Practices and Pitfalls
Mar 2013
Defining Computer System Validation & Software Development Life-Cycle
Feb 2013
Adaptive Clinical Trials - Clinical Trials Version 2.0
Feb 2013
Effectiveness Measures in CAPA and Risk Management Plans: Applying LSS for Quality Metrics
Feb 2013
Social Media: Using The Legal Guideposts to Create Social Media Success (for Healthcare/Lifescience Companies)
Feb 2013
Immunogenicity to biologics: processes, impact on efficacy and safety, and management strategy
Feb 2013
The Toolbox for CAPA and Risk Management
Jan 2013
Basic Cell Culture & Fermentation - Process Development & Manufacture
Jan 2013
Objectionable Microorganisms in Medicinal Products - Aseptic Environment
Jan 2013
Quality Assurance at the (Clinical Research) Site: How to Develop a Manageable Plan
Dec 2012
TM’s world surgery and anesthesiology online conference
Nov 2012
Laboratory Water Systems: Necessary Water Specifications and Validation Challenges
Oct 2012
Risk Assessment-Compliance Using Easy To Fill Out Documentation
Sep 2012
How to Select Best Practices a CRO ?
Sep 2012
Investigator Initiated (Sponsored) Trials – ISSs
Sep 2012
Strategies for Preparing and Submitting Successful Citizen Petitions and Suitability Petitions to FDA
Aug 2012
Site Challenges in Conducting Investigational Device Trials
Aug 2012
TM’s world Pathology & diagnosis online conference
Aug 2012
Sterilization as a Benchmark for Cleaning Validation and Control - Webinar By GlobalCompliancePanel
Aug 2012
Strategic Selection and Development of Immunogenicity Binding Methods
Jul 2012
Software validation and 21 CFR Part 11 remediation planning: FDA inspection strategies
Jul 2012
Specialized Formulations – Biomolecules
Jul 2012
What Every FDA Regulated Company Needs to Know About its FDA District Office
Jul 2012
Project Management for Auditors – Improving audit productivity for GCP, GMP and GLP
Jul 2012
TM’s world Protein & Enzyme online conference
Jul 2012
Clinical Trial Auditing - Identifying risks and building a more compliant and successful trial
Jul 2012
Recommendations for Cell Banks used in GXP testing - Webinar By ComplianceOnline
Jun 2012
TM’s world Neuroscience online conference
Jun 2012
Risk & Benefit Management in Drug Safety
May 2012
Making Sense of FDA’s (proposed) Rules for the Development and Approval of Biosimilars
May 2012
Supplier Controls to Meet Tougher U.S. FDA Requirements
May 2012
Integrating Clinical Evaluation and Risk Management
May 2012
Establishing and following Good Clinical Practice (GCP) compliant with the FDA requirements
May 2012
How to Prepare for FDA BIMO Inspections
May 2012
TM’s annual world microRNAs and RNAi online symposium
May 2012
The Hero of Manufacturing Contamination Control - The Microbiology Lab
Apr 2012
TM’s world Virology & Microbiology online conference
Apr 2012
Life Cycle Validation of GMP Potency Bioassays
Apr 2012
Live webinar on Latin America: Regulatory Compliance Requirements for Life Science Products (Focus: Brazil, Mexico, Argentina) By Compliance2go
Mar 2012
Project Management To Meet CGMP Requirements
Mar 2012
TM’s world Immunology online conference
Mar 2012
Doing Business Despite Embargoes and Sanctions: OFAC Licensing
Mar 2012
Managing Immunogenicity Risk in Biopharmaceuticals
Mar 2012
Method Validation in Drug Development Process - Common Mistakes and Issues
Mar 2012
Software Verification and Validation Planning and Implementation
Mar 2012
Design History Files, Device Master Records, Device History Records, and Technical Files / Design Dossiers -- Differences and Similarities
Feb 2012
Annual Best Practice Phase IV studies
Feb 2012
Live Web Seminar Dietary Supplement Regulatory Compliance in the United States: Labeling, Product Claims & Updates from the FDA By compliance2go
Feb 2012
Introduction to the Electronic Common Technical Document
Jan 2012
Live Web Seminar Design Controls: What to know when it comes to FDA regulated industry? By compliance2go
Jan 2012
Validation and use of Access Databases in FDA regulated environments
Jan 2012
Purposeful Water and Steam System Validation – Not Just A Regulatory Requirement
Jan 2012
How to Format Succinct and Comprehensive 510(k)s and PMAs
Jan 2012
Live Web Seminar China: Compliance Processes for Life Science Products (Company Establishment, Clinical Trials, Registrations, Renewals and Supply Chain Considerations By compliance2go
Jan 2012
Proven Root Cause Investigation Techniques for Pharmaceutical Water Systems
Dec 2011
Live Web Seminar on Managing high-enrolling sites: CRO’s perspective By compliance2go
Dec 2011
Lyophilization Process Development and Cycle Design
Nov 2011
Best Practices in Complaint Management - Webinar by GlobalCompliancePanel
Nov 2011
Drug Master Files (DMFs) - Understanding and Meeting Your Global Regulatory and Processing Responsibilities By compliance2go
Sep 2011
Investigator responsibilities and Legal commitments in Drug and Device Clinical Research
Sep 2011
Common GCP Violations and Site Mistakes - How to Avoid them
Aug 2011
How Due Diligence in Accurate Adverse Event Reporting is the Key to a clean FDA Audit
Aug 2011
How to write Standard Operating Procedures (SOPS) & Work Instructions (Wis) that Meet and Exceed Compliance Requirements
Aug 2011
Clinical Project Management - Webinar By ComplianceOnline
Aug 2011
Creation and management of a Controlled Document System for a Life Sciences manufacturing plant utilizing the principles of Lean Documents and Lean Configuration
Aug 2011
Vendor Qualification - Designing and Implementing an Efficient and Compliant Vendor Program
Aug 2011
Trial Master File for Research Sites: Can You Pass FDA Inspection?
Aug 2011
Vendor Qualification Auditing for FDA Computer System Compliance - Webinar By ComplianceOnline
Jul 2011
Clinical Document Management and Collaborative Electronic Data Exchange in Clinical Trials
Jul 2011
Key Concepts in OSHA Recordkeeping – 2.5 hrs comprehensive webinar
Jul 2011
Navigating the new FDA world of Combination Products
Jun 2011
Risk-Based Validation for GxP Facilities - Webinar By GlobalCompliancePanel
Jun 2011
`The Right Stuff` – Implementing Quality Control Tools in Quality Systems Operations
May 2011
Patient Recruitment & Retention – Challenges & Best Practices
May 2011
ComplianceOnline Virtual Seminar - Controlling Outsourcing Using Quality Principles - For Lifesciences Companies
May 2011
Retirement of Computer Systems: Strategies for FDA Compliance and Tools for Implementation
May 2011
Eliminate the Confusion - New Requirements for Clinical Laboratories to Meet GCP
Apr 2011
Recent Major Industry CGMP Failures
Apr 2011
Presenting the real GCP handbook: Build solid knowledge of GCP by learning the rules exactly as they appear in the official text
Mar 2011
A Comparison of ICH Q-10 Quality System and the FDA’s Quality Systems Approach (QSA) to the Pharmaceutical cGMPs
Mar 2011
How to Prevent or Handle Protocol Deviations and Violations to be GCP and Regulatory Compliant?
Mar 2011
Differences between ICH-GCP and FDA regulations
Mar 2011
Design Control Explained - Medical Device Webinar
Mar 2011
Responsibilities of a Clinical Research Coordinator managing clinical trial/s under the supervision of a Principal Investigator
Mar 2011
Implementation of Rapid Microbiological Methods
Feb 2011
Last changes in Canadian ethics regulations for clinical trial
Feb 2011
How to secure GCP compliance in Clinical Trials: The complete overview of the critical parameters 2010
Feb 2011
Software Verification and Validation Planning and Execution
Feb 2011
Eliminate the Confusion –Annex 13 GMP guide
Feb 2011
Responsibilities of a Principal Investigator in Clinical Trials: What you Must Do to Ensure Trial Compliance
Feb 2011
Validating Excel and Word Applications Documents - Webinar By GlobalCompliancePanel
Feb 2011
Compliance with The European Medicines Agency reflection paper on e-source data
Feb 2011
Analytical Instrument and Equipment Qualification in Quality Laboratories - Webinar By GlobalCompliancePanel
Feb 2011
Risk-Based Verification and Validation Planning to Meet U.S. FDA, ICH Q9 and ISO 14971
Feb 2011
Understanding and Implementing FDA’S 21 CFR Part 11
Feb 2011
Ethics, Standards and Identifying Risks in Clinical Research - ComplianceOnline Clinical Training
Jan 2011
Assessing FDA’s Proposed Changes to the 510(k) Process in
Jan 2011
cGMP: Strategies for implementation and compliance for Phase I Investigational Drug and Biologic products
Jan 2011
How to Vet an IRB: Expose and Fix Problems Before They Threaten Your Trial
Jan 2011
Internal 21CFR Part 11 Compliance Auditing of Computer Systems - Webinar By GlobalCompliancePanel
Jan 2011
Japan - Regulatory Filing Requirements and Compliance Processes for Life Sciences - Part I and Part II - Webinar By GlobalCompliancePanel
Jan 2011
101 cGMP To-Do List for - Webinar By GlobalCompliancePanel
Jan 2011
An Easy to Implement Integrated Risk Management Approach Compliant with ISO 14971
Jan 2011
How to Set up Data Monitoring Committees (DMCs / DSMBs) and what is effect on the Drug Development Process - ComplianceOnline Clinical Training
Dec 2010
The FDA`s Working Group Reports, I & II - New Directions - Webinar By GlobalCompliancePanel
Dec 2010
Assessing GCP Compliance in Clinical Trial Audits- Risk management and Best practices - ComplianceOnline Clinical Training
Dec 2010
QSR Device Inspections – Transition from “Barely Surviving” to “Gaining Control”
Nov 2010
Conducting Clinical Trials in Latin America: keys to successful study implementation
Nov 2010
Best Practices of Recruiting Subjects in Conducting Clinical Trials: What does it take to be successful - ComplianceOnline Clinical Training
Nov 2010
Performing Investigations for Environmental Excursions - ComplianceOnline Biotechnology Training
Nov 2010
How to Use Foreign Trial Data in Your NDA Approval Process
Nov 2010
Are you a new Clinical Research Coordinator? Tips on how to get started, what to expect
Nov 2010
Clinical Trial Regulations and GCP Compliance as they relate to Adverse Events - How to Assess and report AEs and SAEs
Oct 2010
Quality System Regulation (QSR) Management Responsibilities
Oct 2010
Navigating Pediatric Trials from recruitment to successful on-time completion
Oct 2010
Data Monitoring Committees (DMCs) effect on subject safety in clinical research and how to set it up to be effective
Oct 2010
The FDA Tripod - Clinical Trial Regulations, Compliance and GCP in Drug Development
Oct 2010
Ensuring GCP compliance through quality auditing in clinical trial
Sep 2010
The ICF Process: Tips on Achieving Optimal compliance and Comprehension
Sep 2010
EU IMPD vs. US IND: Comparing the Content and Agency Expectations
Sep 2010
What are the “Good Clinical Practices” (GCP) of Research involving Human Subjects
Sep 2010
Developing Supplier Quality Auditor Training Programs
Sep 2010
Effective & Essential CAPA process to avoid FDA 483 - Webinar by GlobalCompliancePanel
Sep 2010

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