Morningside Pharmaceuticals Ltd | Pharmaceutical Company

This is achieved through total dedication to quality and risk management and continual improvement throughout all processes, in order to ensure that quality is maintained until the final product is received and beyond.

Quality Management covers all aspects of what we do and all the standards we maintain including  ISO 9001, EU cGDP and EU cGMP (pharmaceuticals),  ISO 13485 (medical devices), the Medical Device Directive 93/42/EEC as amended, and our Health and Safety practices.

Our commitment to meeting these requirements can be observed throughout all of our systems and procedures where comprehensive Quality Assurance, Quality Control and Registrations are fundamental.

We comply with the relevant aspects of The Misuse of Drugs Act 1971, the Misuse of Drugs Regulations 2001 and the Misuse of Drugs (Safe Custody) Regulations 1973.

We are regularly inspected to ensure that standards are maintained and our quality management system is complete throughout, and our own internal audit processes mean that we maintain and develop our systems in line with the latest legislation and guidelines.