February 9, 2021 | Compliance An Analysis Of MHRA’s Latest Annual GMP Inspection Deficiencies Report Are you aware of recent changes from EMA pertaining to manufacturers of chemically synthesized drugs and biological products? Barbara Unger Principal Consultant 10 Minute Read
February 15, 2018 | Compliance Closing the Gaps: Next Steps in EU MDR Compliance Brian Burns CEO, Validant 3 Minute Read
February 5, 2018 | Compliance Gap Assessments: A Vital First Step to Comply with New EU Medical Device Regulations Brian Burns CEO, Validant 2 Minute Read