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,
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Drugs Licensing & Controlling Authority
(Uttarakhand) s