Taj Pharmaceuticals LICENCES & CERTIFICATES for Pharmaceutical Tablet Plant

  1. WHO-cGMP Certified
    Taj Pharmaceuticals is manufactures with Pharmaceutical Tablet Plant under WHO-cGMP Plant. Taj Pharma is licenced to manufacture Pharmaceutical Tablet Plant formulation from Food and Drug Administration of Indian authorities as the rules and regulations with all compliances for international markets.
  2. ISO 9001: 201     
    All infrastructure of Taj Pharmaceuticals is ISO 9001:201 compliant and Taj Pharma team adheres to the specifies requirements for a quality management system in order to achieve : 1) To demonstrate our ability to consistently provide products and services that meet customer and applicable statutory and regulatory requirements, and. 2) Taj Pharma aims to enhance customer satisfaction through the effective application of the system, including processes for improvement of the system and the assurance of conformity to customer and applicable statutory and regulatory requirements.

All manufacturing units of Taj Pharmaceutical follows the requirements of ISO 9001:201; which are generic under our standard operating procedure (SOP) and we intend such SOPs to be applicable to all manufacturing units, regardless of its type or size, or the products and services we provide.

  • DUN & BRADSTREET (DUN’S NO. 7206112)   
    Taj Pharma is recognised by Dun & Bradstreet; it is a corporation that offers information on commercial credit as well as reports on businesses with Data Universal Numbering System (DUNS numbers.

Third Party / Private Label / Customised Manufacturing

Taj Pharma has excellent infrastructure and drug manufacturing technology to offer private label / third party brands and generics as well; Taj Pharma team invites you to approach us for providing you an option for your products giving your customized requirement from product name to formula; also in international packing and manufacturing standards with all regulatory document needs.

We are exporting our Pharmaceutical Tablet Plant product in Following Countries:- 

Russia and CIS Countries: Azerbaijan, Armenia, Belarus, Georgia, Kazakhstan, Kyrgyzstan, Moldova, Russia, Tajikistan, Turkmenistan, Uzbekistan and Ukraine

GCC/ Middle East Countries: Saudi Arabia, Yemen, Oman, Bahrain, UAE, Lebanon, Jordan, Iraq.

African Countries: Nigeria, Tanzania, Sudan, Zambia, Benin, Angola, Liberia

Southeast Asia: Cambodia, Indonesia, Laos, Malaysia, Myanmar, Philippines, Singapore, Thailand, Vietnam, Brunei Darussalam

Other Asian Countries: Nepal, Myanmar, Malaysia, Cambodia, Bhutan, Sri Lanka, Mauritius

Pharmaceutical Tablet Plant Regulatory Documents:

  1. Certificate of Analysis (COA)
  2. Method of Analysis (MOA)
  3. Stability Data (Accelerated stability / Long term stability / Zone 4b)
  4. CTD Dossier / ACTD Dossiers / eCTD Dossiers
  5. Certificate of Pharmaceuticals Product (COPP)
  6. Free Sale Certificate (FSC)