Quality agreements are necessary to ensure compliance with industry standards and regulations, first and foremost, compliance with legal requirements. The GMP requires manufacturers and importers of medicinal products to take all the necessary steps to guarantee the safety, effectiveness and quality of their products.
GMP defines quality measures for both production and quality control and defines general measures to ensure that processes necessary for production and testing are clearly defined, validated, reviewed, and documented, and that the personnel, premises and materials are suitable for the production of pharmaceuticals and ...
Ing to Boundy (2012), typically, a written contract will include: Date of agreement. Names of parties to the agreement. Preliminary clauses. Defined terms. Main contract clauses. Schedules/appendices and signature provisions (para. 5).
 
                    