Research - Johannesburg, Gauteng, South Africa
Your partner in Evaluation, Monitoring and Regulation of Quality, Risk and Safety activities We understand the complexities of running a Life Sciences BusinessBiomedply is a pioneer in providing Quality Management System and Regulatory Affairs services to life science businesses promoting and enhance Good Manufacturing Practices and Good Documentation Practices to ensure patients receive safe and beneficial sterile products with reduced risk of contamination, infection, or incorrect dosing.We provide services to the pharmaceutical, biologics, sterile compounding, biotechnology, and medical device industries for resolution of compliance and regulatory challenges.As your partners, we can negotiate the potential minefield of regulatory compliance with insight, hindsight, and the clear advantage of our unique expertise and experience.Business Sector:• Medical Device Manufacturing Industry• Primary Packaging Manufacturing Industry• Drug Manufacturers• BiotechnologyServices• Risk Management• Quality Management • Documentation and technical evaluation of medical device procuring processes. • Personnel and Environmental Monitoring of the Cleanroom• Warehouse Quality ManagementOur Company Specialties:• Regulatory Quality and Risk Management Strategy,• Quality Assurance, • Procuring Processes.• Cleanroom Qualification/Monitoring/Validation,• Quality Management System Compliance and Quality Turnkey Services, • Biological Manufacturing Unit Compliance• Medical Device Design and Development We assist medical device companies, pharmaceutical companies and laboratories in catalysing the strategic development in the quality assurance, documentation of validation protocols, reports and standard operating procedures, cleanroom environmental monitoring, warehouse management and risk management. Our team evaluates manufacturing operations, identifies areas for improvement and executes system compliance.