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OUR OFFER
- Audits of registration dossier for medicinal product
- Audits of active substance (API) registration dossier – ASMF, DMF
- Audits of API manufactures and suppliers
- Audits of manufacturers of active substance(s) (API(s)) for use in clinical trials (CTs)
- Audits of manufacturers of (investigational) medicinal products
- Audits of manufacturers of raw materials, finished products and packaging materials suppliers
- Audits of contract laboratories and manufacturers
- Coordination and preparation of manufacturing sites for Authorities/ Agencies and client inspections/audits
In each case, when the service you require is not listed on our website, please Contact us through contact form or by phone, and we will make every efforts to find the satisfactory solution for you.
