
Upcoming Training Courses

CMC Regulatory Compliance for Biologics: A CMC approach to IMPD Walkthrough for Biologics
CMC Regulatory Compliance for Biologics - An IMPD Walkthrough for Biologics

Drug-Device Combination Products: Quality & Regulatory Requirements
Combination Products: Quality & Regulatory Requirements

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.

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.

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.

Development and Validation of Bioassays
Master bioassay development and validation with expert-led training. Gain the tools to ensure potency, precision, and regulatory success.
Testimonials
“Tara presented the material in a very engaging and practical way, using real-life examples that made the concepts easy to understand. She answered many audience questions and ensured the explanations were relevant for the whole group. I particularly appreciated her relaxed delivery and common-sense approach to choosing the right statistical method. The lecturer and the examples were the highlight.”Maria Kadow
Drug Substance Specialist, Scandinavian Biopharma
“I really enjoyed the questions and discussions around the participants’ topics. It expanded on the key points and made it much easier to apply the learning to specific cases.”Lindsey Rios
Senior Scientist I , Arsenal Biosciences
“The comprehensive walkthrough an example product and how it should be approached from the design and risk management control perspective was great.”Magdalena Wierzbicka
Risk Management Specialist, Biocomposites
“Thanks to Symmetric and James, it was a very helpful training to align the different functional areas and levels of knowledge in the right direction. ”T. Person
, Organon
“The knowledge of the trainer, the white board which makes it interactive and alive”Saoudatou Bah
Regulatory Affairs Specialist, Becton Dickinson
“I am very satisfied with the course. The training was extremely valuable, and James's expertise and ability to convey information clearly made the experience engaging and informative. I particularly appreciated the use of real-world examples, which helped contextualize the material and enhance understanding.”Carol Frid
Regulatory Affairs Specialist, Phillips-Medisize A/S
“Very logical way to present complex regulation / requirement Like the use of example”Jennifer Maillard
Compliance Quality Manager / PRRC, Haleon
“Responses to questions were great!”Yewande Odugbesan
Senior Manager Regulatory Compliance, AGC
“I really liked the straightforward way of presenting the material, and there is no doubt that Len knows what he is talking about”Matthias Thorolfsson
Matthias Thorolfsson, Alligator Bioscience
“It has been a well-structured training, with clear and well-explained concepts. I can't say anything negative or anything to improve.”Lorena
R&D Technician, B. BRAUN SURGICAL
“Fantastic training with a good overview on key regulatory topics. I loved the live interactions and the focus on real case scenario situations from the audience.”Alessandro Fammartino
Project Manager, CSEM
“James demonstrated deep subject-matter expertise and presented complex regulatory concepts in a clear and structured manner. The course was well-paced, with a good balance between theoretical content and practical insights. Thank you!”Halina Thivolle
Regulatory Affairs Manager,
“James provided practical and evidence supported materials that will help our team on next steps for implementing AI in our quality Systems”Julie Underdahl
Principal Regulatory Affairs Specialist, AliveDX
“Tara presented the material in a very engaging and practical way, using real-life examples that made the concepts easy to understand. She answered many audience questions and ensured the explanations were relevant for the whole group. I particularly appreciated her relaxed delivery and common-sense approach to choosing the right statistical method. The lecturer and the examples were the highlight.”Maria Kadow
Drug Substance Specialist, Scandinavian Biopharma
“I really enjoyed the questions and discussions around the participants’ topics. It expanded on the key points and made it much easier to apply the learning to specific cases.”Lindsey Rios
Senior Scientist I , Arsenal Biosciences
“The comprehensive walkthrough an example product and how it should be approached from the design and risk management control perspective was great.”Magdalena Wierzbicka
Risk Management Specialist, Biocomposites
“Thanks to Symmetric and James, it was a very helpful training to align the different functional areas and levels of knowledge in the right direction. ”T. Person
, Organon
“The knowledge of the trainer, the white board which makes it interactive and alive”Saoudatou Bah
Regulatory Affairs Specialist, Becton Dickinson
“I am very satisfied with the course. The training was extremely valuable, and James's expertise and ability to convey information clearly made the experience engaging and informative. I particularly appreciated the use of real-world examples, which helped contextualize the material and enhance understanding.”Carol Frid
Regulatory Affairs Specialist, Phillips-Medisize A/S
“Very logical way to present complex regulation / requirement Like the use of example”Jennifer Maillard
Compliance Quality Manager / PRRC, Haleon
“Responses to questions were great!”Yewande Odugbesan
Senior Manager Regulatory Compliance, AGC
“I really liked the straightforward way of presenting the material, and there is no doubt that Len knows what he is talking about”Matthias Thorolfsson
Matthias Thorolfsson, Alligator Bioscience
“It has been a well-structured training, with clear and well-explained concepts. I can't say anything negative or anything to improve.”Lorena
R&D Technician, B. BRAUN SURGICAL
“Fantastic training with a good overview on key regulatory topics. I loved the live interactions and the focus on real case scenario situations from the audience.”Alessandro Fammartino
Project Manager, CSEM
“James demonstrated deep subject-matter expertise and presented complex regulatory concepts in a clear and structured manner. The course was well-paced, with a good balance between theoretical content and practical insights. Thank you!”Halina Thivolle
Regulatory Affairs Manager,
“James provided practical and evidence supported materials that will help our team on next steps for implementing AI in our quality Systems”Julie Underdahl
Principal Regulatory Affairs Specialist, AliveDX
Clients that have benefited from our courses




























