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We offer a wide range of courses for organizations, auditors and inspectors – on site or online. Built by industry experts, our PCPC training portfolio provides a holistic experience that covers all the important topics such as:
Gain the essential skills and knowledge in the field of pharma, cosmetics, & personal care
Introduction to 21 CFR 210 / 211 GMP's for Finished Pharmaceuticals Training
During this interactive training, learn to implement GMP principles for cosmetic ingredient manufacture as part of the quality management system. Participants will understand how to implement an EFfCI compliant quality management system.
During this interactive training, learn to interpret and apply the FDA requirements for production, quality systems and management of finished pharmaceuticals: 21 CFR 210 and 211. Discuss ways to minimize or eliminate issues related to contamination, mix-ups, superpotency/subpotency, misbranding, bio-availability, and safety and efficacy.
Contact us for more information or take a look below for more details on these courses.
This training covers the ICH Q7 GMP's for Active Pharmaceutical Ingredients. Learn the requirements for manufacture, control, packaging and testing of Active Pharmaceutical Ingredients (API's) and how to reduce or eliminate the risk of inconsistencies and contamination in API's.
Introduction to EFfCI Training
Introduction to GMP for Active Pharmaceutical Ingredients ICH Q7/EXCiPACT Training
We are the world’s leading provider of testing, inspection and certification services. We are recognized as the global benchmark for sustainability, quality, and integrity. Our 99,600 employees operate a network of 2,600 offices and laboratories, working together to enable a better, safer and more interconnected world.
Introduction to ISO 22716:2007 GMP for Cosmetics Training
Through a series of discussion-based sessions and interactive workshops, learn how to help your organization demonstrate Good Manufacturing Practice (GMP) compliance using ISO 22716. Build a strong foundation of knowledge and skills.
Through interactive workshops and audit role play, participants will learn how to audit Cosmetics GMP’s according to ISO 22716:2007 and ISO 19011:2011 guidance.
Learn to perform an internal audit of part of a LMS based on ISO/IEC 17025:2017 (or equivalent) and report on the effective implementation and maintenance of the management system in accordance with ISO 19011.
Introduction to ISO/IEC 17025:2017
The purpose of this course is to equip learners with a general overview and understanding of the requirements of ISO/IEC 17025:2017.
Through a series of interactive sessions and hands-on workshops, ensure compliance by becoming familiar with the World Health Organization (WHO) Good Distribution Practices (GDP) for Pharmaceutical Products.
This introductory course provides an overview of Good Laboratory Practices (GLP) and their importance in ensuring data integrity, regulatory compliance, and reliable laboratory results in GMP-regulated industries.
Introduction to Good Documentation Practices (GDP)
This introductory course provides an overview of Good Documentation Practices (GDP) and their importance in maintaining compliance, ensuring data integrity, and supporting regulatory requirements across GMP/GDP-regulated industries.