Clear documentation requests help both parties understand what needs to be reviewed before evaluation or supply. PERACI coordinates requests for product and source-specific information; availability and disclosure conditions are confirmed individually.
Product and safety information
You may request a specification, certificate of analysis (COA), safety data sheet (SDS), or packaging and storage information. The document version, source and relevance to a proposed material must be checked. A representative COA is not a substitute for the batch-specific document associated with an agreed supply.
Regulatory documents
GMP evidence, Written Confirmation (WC), Drug Master File (DMF) information, Letters of Access (LOA) or Certificates of Suitability (CEP) may be relevant to a project. We do not represent these as available for every product. Applicability, holder, validity, access conditions and target-market requirements must be confirmed for the particular manufacturer and material.
What to include in your request
- Product name and CAS number, if known.
- Required grade or standard and intended use.
- Destination market and requested document type.
- Your company, evaluation stage and any relevant deadline.
Responsible handling
Third-party documents may be subject to confidentiality and distribution restrictions. Sensitive files are not automatically published on this website. Manufacturer identities, signatures and certification ownership must remain accurate.