Our associate's technical expertise and outstanding project execution enables us to assist local and multi-national pharmaceutical and biotechnology clients to significantly improve operational capabilities and process control., optimize cost and minimize risk. We specialize in complying with FDA and EU current good manufacturing practice (cGMP) and international regulatory guidelines to help launch new products in the market.
• Concept Note, Planning and Process Design.
• Comply with WHO/USFDA/MHRA/MCC/PICS/1CH guidelines with
• Expertise in Tablet/Injection/Liquid Oral/Parental/Interments/Aerosol/Soft Gelatin.
• Documentation /Qualifications/Validations/Process Validation/SOPs etc.
• Audit Assistance