Training Courses
Browse our comprehensive list of pharmaceutical and biotech training courses.
Process Scale-up & Tech Transfer for Injectables
Certified 3-day online course in live interactive format with case studies on sterile injectables manufacturing.
CMC Strategy for Biologics: Building a Submission-Ready IMPD
CMC Regulatory Compliance for Biologics - An IMPD Walkthrough for Biologics
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.
Quality Requirements for Biologics
Take a deep dive into the world of biologics and intensify your know-how about the Quality & GMP requirements.
Statistical Methods Across the Product/ Process Lifecycle
Apply statistical methods across the product lifecycle. Learn data analysis, process control, and regulatory compliance.
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.
Quality Requirements for Solids
Register for Symmetric 3-day pharma online course to obtain detailed information about the manufacturing and quality characteristics of solids
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
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 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.
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.
Process Scale-up, Validation & Technology Transfer
Certified 3-day online course on pharmaceutical process validation, scale-up of manufacturing processes and technology transfer.
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.
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
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.
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.
CMC and Regulatory Requirements for Inhalation Drug Products
CMC regulatory requirements for inhalation drug products.