Who Certificate

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OFFICE OF THE DRUGS CONTROLLING & LICENSING AUTHORITY Directorate General of Medical Health & Family Welfare, Sahastradhara Road, Dehradun (Uttarakhand) F.no.17P//37 /2005/ "769 Date: 6 Y June 2016 Certificate of Good Manufacturing Practices Certificate no.:17P/1/37/2005/1320 On the basis of the inspection carried out on 02.06.2016 we certify that the site indicated on this certificate complies with Good Manufacturing Practices for the dosage forms, categories and activities listed in Table 1. 1. Name & Address of site: Ms Synokem Pharmaceuticals Ltd. Plot No. 35-36, Sector-64, IIE, Ranipur, Haridwar, Uttarakhand, 2. Manufacturer's license number: Form 25- 19/UA/2005 Form 28- 17/UA/SC/P-2005 3. Table 1: - Dosage form(s) Category(ies) Acctivity(ies) Tablets ‘Non betalactum, Manufacturing Capsules (Hard ‘Non betalactum, ‘Manufacturing Gelatin) ‘Oral Liquid ‘Non beta Tactum, ‘Manufacturing Tablets(Hard Gelatin) | Hormone ‘Manufacturing Capsule The responsibility for the quality of the individual batches of the pharmaceutical products manufactured through this process lies with the manufacturer. This certificate remains valid until 05.05.2018. It becomes invalid if the activities and/or categories certified herewith are changed or if the site is no longer considered to be in compliance with GMP. The firm is following Good Manufacturing Practices as per World Health Organiazation(WHO)TRS Guide Lines, in the Manufacturing & testing of the said categories of Products and Items in respect of which the Certificates of Pharmaceuticals products have been issued. Address of certifying Authority: Directorate General of Medical Health & Family Welfare, Sahastradhara Road, Dehradun (Uttarakhand) INDIA. Name & function of responsible person: Shri Tajber Singh Drugs Licensing & Controlling Authority Uttarakhand. Email: descaling Tel.no. NA Fax. no. 0135260874, ae Drugs Licensing & Controlling Authority (Uttarakhand) s

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