Good manufacturing Practices (GMP) is a quality system for the manufacturing of medications in the pharmaceutical industry and is considered the “gold” standard of quality systems of this type.
BioPlan's Staffs are Expert in Designing New and Managing Ongoing GMP Quality Systems Including:
Pharmaceutical Warehouses
QP Batch release of imported pharmaceuticals
Early Pharmaceutical Manufacture
Pharmaceutical Warehouses
QP Batch release of imported pharmaceuticals
Early Pharmaceutical Manufacture
Management and conducting of internal audits.
Required performing of audits of your global suppliers.
BioPlan will Provide for You and Your GMP System, Including Managing the Following:
Controlled Documentation System
Training for you, your management, and your staff
Management and negotiation with the Israeli MoH GMP department
Obtaining GMP certification
Control of the deviation system
Change Control management
CAPA management
Management Review
Risk Management
Development and management of a system to check and follow all updated printed materials (inserts and labels)
Vendor Approval
Mock Recall and Recall management
Internal and External Audits
Support and presence at auditing for you, for your site and system
Provision of professional on-going services and support