Anna Sahlholm
Anna Sahlholm is employed at GBA Key2Compliance and has more than 15 years of experience from product and process development in close collaboration with research and within the medical device industry. Anna has worked with research, product development, strategic product management, clinical evaluations, processes for traceability, risk management, quality, and regulatory compliance for a variety […]
Kristine Frederiksen
Medicines Inspector at Danish Medicines Agency (DKMA) Kristine is a Medicines Inspector at DKMA, she is specialized in inspection of companies working under GMP, GDP and CAN standards. She has been at the Danish Medicines Agency for 6 years. Before that she worked in different companies in the pharmaceutical industry for +10 years. She holds […]
Thomas Noe Vestergaard Pedersen
Team manager and Medicines Inspector at Danish Medicines Agency (DKMA) Thomas is a Team Manager for a team of 18 medicines inspector at DKMA. He has been at the Danish Medicines Agency for 9 years. Before that, he worked for +10 years in different pharmaceutical companies. He holds a Ph. D. degree in Exotoxicology and […]
Björn Hammarberg
Ph.D. (Biochem.), Post Doc.(Biochem. Eng.), Dipl. BA (Intl. Marketing) Managing Director, Chairman & Founder, ABD Life Sciences Ltd Björn is an entrepreneur with job experience in several areas of the Life Science industry, including R&D, business development and marketing & sales. Björn has worked in a wide diversity of fields, among them molecular biology, molecular diagnostics, bioprocessing, […]
Nina Bjork
Nina Bjork is passionate about helping organizations realise and overcome the barriers to sustainable long-term growth. She brings over 20 years’ experience across a range of pharmaceutical companies and from the Regulatory Authorities. She has worked in small, medium and large pharma biotech companies across the product lifecycle for a wide range of dosage forms. […]
Laurence O’Leary
Laurence is Founder of ValidEire ApS and has over 20 years working in Pharmaceuticals and Medical Devices. Laurence has a long‐ track experience in QA, Compliance, Cleaning Validation and Process Validation roles. He presently works as a Contract Validation Specialist. He is a seasoned trainer inhouse for all of his previous clients in Compliance subjects […]
James L. Vesper
Dr James L. Vesper designs and develops instructional courses and workshops for the pharmaceutical industry. He established and is president of the firm, LearningPlus, Inc., and has had more than 25 years’ experience in the pharmaceutical industry. Dr Vesper worked eleven years at Eli Lilly and Company, Indianapolis. His last assignment was as Project Leader […]
Energy Kristina Hansen
Energy Kristina Hansen is the founder of MilCor Consulting. She is an accomplished speaker and presenter who is known for her warmth, humour, and energy in her motivational presentations. Energy Kristina is also an annual guest lecturer on the topic of ‘Changing Undesirable Behaviours’ at the University of Copenhagen (LIFE) since 2013. She has trained […]
John Y. Lee
John Y. Lee is Executive Director of Pharmaceutical Compliance Associates, an organization specializing in pharmaceutical compliance consulting, auditing, quality assurance, validation, and training. Prior to joining PCA, Mr. Lee held positions as Quality Assurance and Quality Control Director at Altana, Inc., Melville, New York; Quality Assurance Manager at Organon, Inc., West Orange, New Jersey; GMP […]
Peter L. Knepell
Dr Pete Knepell is president of Peak Quality Services in Colorado Springs, CO. Since 1988 he has trained thousands of professionals in quality systems and quality improvement methodologies. His past clients include: several defence agencies, the Canadian Red Cross, Sony, Corning, Texas Instruments, Xerox, Hewlett Packard, Heritage Valley Health System, GlaxoSmithKline, Amgen, GE Healthcare, Roche […]