Training Courses
Browse our comprehensive list of pharmaceutical and biotech training courses.
Design Control and Risk Management For Combination Products
Combination Products: Quality & Regulatory Requirements
Process Scale-up & Tech Transfer for Injectables
Certified 3-day online course in live interactive format with case studies on sterile injectables manufacturing.
AI Systems in Quality & Regulatory Affairs
Discover how AI is transforming Quality and Regulatory Affairs in this 3-day online training. Learn from industry expert James Pink how to apply AI to regulatory intelligence, submissions, QMS, and auditing while meeting FDA, EU, and ISO 42001 requirements.
CMC Strategy for Biologics: Building a Submission-Ready IMPD
CMC Regulatory Compliance for Biologics - An IMPD Walkthrough for Biologics
Drug-Device Combination Products: Quality & Regulatory Requirements
Combination Products: Quality & Regulatory Requirements
CMC for Antibody-Drug Conjugates: Strategies for Successful Development and Manufacturing
Practical training on ADC CMC development, manufacturing, regulatory expectations, and lifecycle control. Led by Dr. Len Pattenden.
Development and Validation of Bioassays
Master bioassay development and validation with expert-led training. Gain the tools to ensure potency, precision, and regulatory success.
VHP/vH2O2 Bio-Decontamination Master Class
Learn to develop, qualify, and troubleshoot VHP bio-decontamination cycles in line with Annex 1, ICH Q9(R1), and global GMP expectations.
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Advanced CMO Management: Selection, Qualification, and Operational Excellence
Practical frameworks for performance monitoring, risk-based oversight, and continuous improvement across multiple partners and geographies.
AI Systems as Medical Devices
AI-enabled medical devices are now being assessed through multiple overlapping lenses: medical device regulations (EU MDR/IVDR, FDA frameworks), emerging horizontal regulation (EU AI Act), and rapidly evolving expectations for clinical safety, lifecycle control, and transparency. This 3-day live online training focuses on what teams need to implement to build, document, and maintain AI systems that can withstand review — from defining intended purpose and classification, through design control and risk management, to QMS integration and post-market oversight. The sessions are designed for cross-functional alignment: regulatory, QA, clinical, design, and technical stakeholders leave with a shared view of terminology, responsibilities, and evidence expectations.
Mitigating Immunogenicity Risk
Understand strategies for mitigating immunogenicity risk in biopharmaceuticals. Focus on guidelines, risk assessment, and best practices.
Quality Requirements for Biologics
Take a deep dive into the world of biologics and intensify your know-how about the Quality & GMP requirements.
Good Manufacturing Practices in API Production: How to Implement ICHQ7
Learn to implement ICHQ7 for API production. Focus on GMP compliance, risk management, and quality systems.
Stability Testing of Biological Drug Products
Master the stability testing of biological products with this 3-day online course. Learn regulatory guidance, analytical methods, and more.
Real-World Evidence in Rare Diseases: Accelerating Market Access
Learn how to leverage patient-centric real-world evidence (RWE) to accelerate the patient and market access of orphan drugs.
Advanced Industrial Process and Unit Operations Scale-up
This online certification course with case studies and workshops will address success factors for process innovation and scale-up.
Advancing Real-World Evidence Generation for Causal Inference
Review the most current Real-world Evidence guidance, tools, and good research practices and discuss the applications of causal RWE.
Development of Generic Solid Immediate Release Dosage Forms / Formulation and Analytical Method Development
Symmetric pharma in-house training course focusing on generic drug development program, the importance of API and the challenge of QbD.
Pharmaceutical Quality: QRM, CAPA & Root Cause Analysis
Working in quality control in pharma? Join Symmetric course to discover CAPA audit expectations, RCA techniques and application of QRM.
Dissolution Testing, Equipment Requirements, Quality Control & Biowaivers
Online course on dissolution testing, dissolution guidelines, dissolution equipment and pharmacokinetics.
Specifications for Small Molecule Drug Products
Understand the importance of specifications in chemical drug products. Learn to develop and manage product specifications for regulatory compliance.
Statistical Methods Across the Product/ Process Lifecycle
Apply statistical methods across the product lifecycle. Learn data analysis, process control, and regulatory compliance.
Value Added Medicines / Scientific, Regulatory and IP Analysis
Explore the evolving area of Value Added Medicines: innovative generic business development, drug repositioning and market access.
Mastery in mRNA Manufacturing: Navigating International Regulations & Best Practices
Register for Symmetric 3-day pharma online course to explore key steps in the mRNA manufacturing process including new GMP requirements.
Equipment Lifecycle Management
a deep dive into the lifecycle of pharmaceutical equipment for different dosage forms
Pricing and Market Access of ATMPs
Discuss the challenges and opportunities for the commercialization of Advanced Therapy Medicinal Products (ATMPs).
Pharma & Biotech Stability Testing
Understand stability testing for pharmaceutical and biotech products. Learn guidelines, methods, and data interpretation.
Quality Requirements for Solids
Register for Symmetric 3-day pharma online course to obtain detailed information about the manufacturing and quality characteristics of solids
Strategic Marketing for CDMO Industry
Enhance marketing skills in the CDMO industry. Learn market analysis, customer engagement, and branding for CDMOs.
Development of Solid Generic Formulations
Certified 2-day online course in live Interactive format with practical case studies on generic solid dosage forms.
Aseptic Fill & Finish Excellence - Annex 1 Compliance and CFD Insights
Learn about best practices in biological product aseptic manufacturing, fill & finish, contamination control and monitoring.
Technology Transfer for Pharma & Biotech
Certified 3-day online course in live interactive format explores real-world situations and challenges of Technology Transfer
Annex 1 Compliance: Challenges, Solutions and International Impact (EU GMP & PIC/S)
Learn about EU GMP & PIC/S Annex 1 Challenges & Solutions to Compliance
Dissolution Testing and Biowaivers
This three-day online course covers both the theory and practical aspects of pharmaceutical dissolution testing for solid oral dosage forms.
Cleaning Validation in Pharma
Pharmaceutical cleaning validation course on GMP requirements, cleaning validation protocol, sampling techniques and recovery studies.
Paediatric Drug Development & Clinical Trials
Learn online about paediatric clinical trial guidelines, challenges, patient recruitment and ethical issues.
Storytelling and Thought Leadership: Tactics for CDMO Marketing
Enhance your marketing skills in the CDMO industry. Learn about storytelling, thought leadership, customer engagement, and branding for CDMOs.
Stability Testing for Biologics
For professionals involved in biologics development, manufacturing, and quality assurance
Orphan Drugs Clinical Trials
Explore orphan drugs regulatory guidance and clinical trials strategies with EMA professional Dr. Simon Day. Certificate after completion.
CMC Regulatory Compliance for ATMPs
3-days of online training with Dr. Len Pattenden on CMC-compliant regulatory practices for ATMPs.
Process Scale-up, Validation and Technology Transfer for Medical Devices
Join medical devices online course with certificate and gain practical tools for process risk assessment during scale up of medical devices.
Human Factors for Combination Products
Apply user-centered design principles to the development of combination products. The agenda covers all stages of documentation, risk management, design control and regulatory submissions.
Clinical Investigations and Evaluation for Medical Devices
Understand clinical evaluation process including regulatory requirements, the principles of clinical evaluation and study design.
Process Scale-up, Validation and Technology Transfer for Biologics
3-day pharmaceutical online training on scale-up of biologics manufacturing, pharma tech transfer and validation.
CMC Regulatory Requirements for Biosimilars
3-days of online training with Dr. Len Pattenden on CMC-compliant regulatory practices and quality assurance for biosimilars.
PK and ADA Assays for Biologics
Expert-led PK and ADA assay training covering regulatory updates, method development, troubleshooting, and advanced techniques for biologics.
CMC Module in Regulatory Submissions
Certified 2-day online course in live interactive format covering CMC Module in Regulatory Submissions - Online Course
Statistics for Non-Statisticians
Learn practical statistics for quality, manufacturing, and R&D with hands-on training in DOE, ANOVA, regression, and process capability.
Bioequivalence and IVIVC
Join our unique bioequivalence online training focusing on in vitro in vivo correlation, biowaiver guidelines and bioavailability.
GMP Investigations and Problem Solving
The training provides a structured overview of GMP Investigations and Problem Solving to overcome the problems in QA/QC by practical tips.
GCP & Data Integrity for Analytical Laboratories – ICH E6 R3 in Practice
This training will help you to grasp the application of ICH E6 R3 to analytical labs with GCP expectations for audits and sponsors.
Process Scale-up, Validation & Technology Transfer
Certified 3-day online course on pharmaceutical process validation, scale-up of manufacturing processes and technology transfer.
Commercial Functions for CDMOs
Explore the vital role of Sales and other Commercial Functions in today’s heavily fragmented and fiercely competitive CDMO market.
Drug-Device Combination Products: Notified Body Opinion Process
Drug-Device Combination Products: NBOp
Process Development of Solid Dosage Formulations
This 2-day training course will focus on the challenges of solid dosage forms development establishing an effective drug development program.
Contamination Control Strategy
EDIT METhis training covers a systematic evaluation of the requirements of the Contamination Control Strategy as detailed in the EU Annex 1.
Biometrics in Clinical Trials
Overview of Biometrics in Clinical Trials, focusing on data management, statistical programming, and the use of eClinical systems.
CMC/Regulatory Affairs for Nucleic Acids
This 3-day online course with Dr. Len Pattenden provides a deep dive into the critical aspects of CMC and Regulatory Affairs of nucleic acids
Analytical Method Development and Validation
Learn how to apply ICH Q14, Q2(R2), and USP to develop, validate, and manage analytical methods across their lifecycle.
Advanced Strategies and Future Trends in GMP Auditing
Enhance GMP auditing skills with real-world case studies, global compliance insights, and workshops focused on quality and improvement.
Mastering Projects and Regulatory Milestones in Generic Drug Development
Join Symmetric online course and gain necessary soft and hard skills to successfully manage a project in generic pharmaceuticals.
Lipid Based Formulations
Explore the principles behind lipid-based formulations and delve into other topics such as modified and targeted release mechanisms.
CMC Statistics
Live online CMC Statistics training for pharma professionals—apply key statistical tools for validation, methods, and regulatory success.
Aseptic Processing in Manufacture of Sterile Products and ATMPs
Master aseptic processing and Annex 1 compliance in this expert-led training. Boost your GMP skills for sterile and ATMP manufacturing.
Extractables & Leachables Control Strategies
Gain practical skills in extractables and leachables risk assessment, study design, and regulatory compliance in this expert-led E&L training.
CMO Contracting, Oversight and Value Optimisation
Join this expert-led CMO training to master contracting, oversight, and value optimisation, learning practical tools, KPI development, governance models, case studies, and proven strategies to build stronger partnerships and maximise value from your outsourcing agreements.
CMC and Regulatory Requirements for Inhalation Drug Products
CMC regulatory requirements for inhalation drug products.