We can work with you to assess and facilitate Good Manufacturing Practice (GMP) compliance of operations at both your and any partner facilities from Active Pharmaceutical Ingredient (API) Manufacture to Commercial manufacture, testing and packaging.
We are able to conduct any necessary QP audits and provide audit reports as required. We will work with the facilities to close out any observations and then we will provide an audit certificate to support your QP Declaration and/or external vendor management programme.
We hold MHRA licenses for the secondary packaging & assembly of human and veterinary medicines.
We also hold ISO 13485 accreditation for the assembly and packaging of medical devices and in addition we hold ISO 9001 accreditation.
If you’re looking to reduce costs without compromising quality, flexibility and service, we believe Springdew offers you a genuine alternative.
Talk to our team on 01639 849 676 or email firstname.lastname@example.org or fill in the form and we will get back to you as soon as we can. Office hours are Monday to Friday 09:00 to 17:00.