Manufacturing
Novopharm provides you with a full-service CDMO solution. The process begins with formulation and process development, where the CDMO works to optimize the drug’s stability, efficacy, and manufacturability. Once the process is established, we will scale up production while adhering to strict Good Manufacturing Practices (GMP), ensuring quality control, consistency, and regulatory compliance throughout. This includes sourcing raw materials, managing production, performing in-process testing, and maintaining detailed documentation for audits and inspections. By outsourcing to a CDMO, pharmaceutical companies can leverage specialized expertise, reduce costs, and accelerate time to market, while maintaining high standards of product safety and regulatory compliance
Production lines
Diverse traditional and modern production lines and advanced technology produce many different dosage forms, helping to optimize production time while still ensuring product quality.
– BFS
– BOV
– Cream, gel
– Suppositories
– Liquid sachet
– Powder/Gramules/ Hard capsules
– Spray products
Benefits
– Quality control in accordance with GMP and ISO standards: comprehensive testing of finished and semi-finished products
– Competitive rates
– Short lead time
– Design products according to desired selling prices
– Free samples
