The client is a European company that is a global market leader in high barrier laminates to the Transdermal Delivery System market segment offering a broad standard range of laminates.
Client was looking for a partner in china that can register a DMF of their packaging material, the transdermal delivery system used for drugs presented in dermal patches in China.
GRP has offices in Shanghai and Beijing with a full team of regulatory affairs professionals who has many years of experience in DMF of packaging materials, excipients and API registration in china. GRP has established an efficient checklist for the regulatory deliverables of DMF registration in china. The checklist was shared with the client to communicate the list of required documents and it was used also to track the deliverables of the project.