
Upcoming Training Courses

Combination Products
Medical Devices
Design Control and Risk Management For Combination Products
Combination Products: Quality & Regulatory Requirements
8 β 10 September 2026
Online

Scale up
CMC
Pharma & Biotech
Process Scale-up & Tech Transfer for Injectables
Certified 3-day online course in live interactive format with case studies on sterile injectables manufacturing.
13 β 15 October 2026
Online

Medical Devices
Combination Products
Artificial Inteligence
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.
13 β 15 October 2026
Online

CMC
Pharma & Biotech
CMC Strategy for Biologics: Building a Submission-Ready IMPD
CMC Regulatory Compliance for Biologics - An IMPD Walkthrough for Biologics
14 β 16 October 2026
Online

Medical Devices
Combination Products
Drug-Device Combination Products: Quality & Regulatory Requirements
Combination Products: Quality & Regulatory Requirements
4 β 6 November 2026
Online

CMC
Pharma & Biotech
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.
2 β 4 December 2026
Online
Testimonials
βThe in-house training was very detailed and well received by our participants. We received very positive feedback from the team, and the session delivered strong value for our organisation.βDarren McConnon
QC Operational Planner, SGS
βGreat course β well balanced, engaging, and highly relevant to both my current role and long-term career development. The speaker was very experienced, and the programme provided valuable practical guidance for the management of CMOs.βSilvia Lissoni
Technical Operations Director, DOC Generici
βTara 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.βMaria Kadow
Drug Substance Specialist, Scandinavian Biopharma
βI really enjoyed the questions and discussions around the participantsβ topics. It expanded on the key points and made it much easier to apply the learning to specific cases.βLindsey Rios
Senior Scientist I , Arsenal Biosciences
βThe comprehensive walkthrough an example product and how it should be approached from the design and risk management control perspective was great.βMagdalena Wierzbicka
Risk Management Specialist, Biocomposites
βThanks to Symmetric and James, it was a very helpful training to align the different functional areas and levels of knowledge in the right direction. βT. Person
, Organon
βThe knowledge of the trainer, the white board which makes it interactive and aliveβSaoudatou Bah
Regulatory Affairs Specialist, Becton Dickinson
βI 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.βCarol Frid
Regulatory Affairs Specialist, Phillips-Medisize A/S
βVery logical way to present complex regulation / requirement Like the use of exampleβJennifer Maillard
Compliance Quality Manager / PRRC, Haleon
βResponses to questions were great!βYewande Odugbesan
Senior Manager Regulatory Compliance, AGC
βI really liked the straightforward way of presenting the material, and there is no doubt that Len knows what he is talking aboutβMatthias Thorolfsson
Matthias Thorolfsson, Alligator Bioscience
βIt has been a well-structured training, with clear and well-explained concepts. I can't say anything negative or anything to improve.βLorena
R&D Technician, B. BRAUN SURGICAL
βFantastic 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.βAlessandro Fammartino
Project Manager, CSEM
βJames 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!βHalina Thivolle
Regulatory Affairs Manager,
βJames provided practical and evidence supported materials that will help our team on next steps for implementing AI in our quality SystemsβJulie Underdahl
Principal Regulatory Affairs Specialist, AliveDX
βThe in-house training was very detailed and well received by our participants. We received very positive feedback from the team, and the session delivered strong value for our organisation.βDarren McConnon
QC Operational Planner, SGS
βGreat course β well balanced, engaging, and highly relevant to both my current role and long-term career development. The speaker was very experienced, and the programme provided valuable practical guidance for the management of CMOs.βSilvia Lissoni
Technical Operations Director, DOC Generici
βTara 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.βMaria Kadow
Drug Substance Specialist, Scandinavian Biopharma
βI really enjoyed the questions and discussions around the participantsβ topics. It expanded on the key points and made it much easier to apply the learning to specific cases.βLindsey Rios
Senior Scientist I , Arsenal Biosciences
βThe comprehensive walkthrough an example product and how it should be approached from the design and risk management control perspective was great.βMagdalena Wierzbicka
Risk Management Specialist, Biocomposites
βThanks to Symmetric and James, it was a very helpful training to align the different functional areas and levels of knowledge in the right direction. βT. Person
, Organon
βThe knowledge of the trainer, the white board which makes it interactive and aliveβSaoudatou Bah
Regulatory Affairs Specialist, Becton Dickinson
βI 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.βCarol Frid
Regulatory Affairs Specialist, Phillips-Medisize A/S
βVery logical way to present complex regulation / requirement Like the use of exampleβJennifer Maillard
Compliance Quality Manager / PRRC, Haleon
βResponses to questions were great!βYewande Odugbesan
Senior Manager Regulatory Compliance, AGC
βI really liked the straightforward way of presenting the material, and there is no doubt that Len knows what he is talking aboutβMatthias Thorolfsson
Matthias Thorolfsson, Alligator Bioscience
βIt has been a well-structured training, with clear and well-explained concepts. I can't say anything negative or anything to improve.βLorena
R&D Technician, B. BRAUN SURGICAL
βFantastic 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.βAlessandro Fammartino
Project Manager, CSEM
βJames 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!βHalina Thivolle
Regulatory Affairs Manager,
βJames provided practical and evidence supported materials that will help our team on next steps for implementing AI in our quality SystemsβJulie Underdahl
Principal Regulatory Affairs Specialist, AliveDX
Clients that have benefited from our courses




























