How to Start Food and Dietary Supplement Company? FSSAI Registration and Licensing for Food business Operators.
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- by Ajay Kamboj
FSSAI has made mandatory for all food business operators whether they are manufacturer or marketer or distributor/supplier/retailer to take license or register them online under FSSAI portal. Manufacturing companies have to take license of manufacturing under state licensing or central licensing system. Marketing companies need to register only under their portal. If pharma companies or […]
Read MoreHow can a BAMS Doctor Start Ayurvedic Manufacturing Company?
- by Ajay Kamboj
One of our youtube viewer asked us about How a BAMS doctor can start Ayurvedic Manufacturing Company. Requirement for starting a ayurvedic manufacturing company is same as we have discussed in our article: How to start Ayurvedic Manufacturing Company? but this article is specific for Bachelor of Ayurveda, Medicine and Surgery (BAMS) doctors. An Ayurvedic Manufacturing […]
Read MoreRequirements for Ayurveda, Sidha and Unani Quality Control Section: Equipment, Area etc.
- by Ajay Kamboj
Every Ayurvedic, Sidha and Unani manufacturing unit is required to set-up own quality control section or testing should be done through government approved testing laboratory. Tests should be conducted at per Ayurveda, Sidha and Unani pharmacopoeial standard. If tests are not available, tests should be performed under in-house specification or other information available. Work of […]
Read MoreLicense required to manufacture Diabetic Powder
- by Ajay Kamboj
Query: Hi thereI have just seen your video on youtube on Ayurvedic manufacturing etc., which is very helpfulThe reason I am writing to you is to inquire about a different kind of a licence and requirement. I will explain in detail so you can advice me. Well, I have made a Ayurvedic churn for Diabetes, […]
Read MoreHow to start Pharmaceutical Manufacturing Unit in South Africa?
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- by Ajay Kamboj
In this post, we will discuss about how to start Pharmaceutical Manufacturing Unit in South Africa. Topics Cover in this post are Steps before Starting Requirements Sections Procedure Documents Required Pharmaceutical Manufacturing Unit/Company Licensing and Registration is covered under MEDICINES AND RELATED SUBSTANCES ACT, 1965. Medicines Control Council Handles all process related to registration and licensing […]
Read MoreHow to Start Pharmaceutical Manufacturing Unit in Pakistan?
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- by Ajay Kamboj
Procedure for Grant of Drugs Manufacturing License in Pakistan In this article, we will discuss about how to start Pharmaceutical Manufacturing Unit in Pakistan. The Drugs Act, 1976 of Pakistan regulates the import, export, manufacture, storage, distribution and sale drugs in Pakistan. The grant of licenses to manufacture drugs is regulated by Central Licensing Board […]
Read MoreSite Master File for Manufacturing Units for Pharmaceutical Industry
- by Ajay Kamboj
Manufacturer Licensee has to submit site plan of manufacturing premises to drug authority along with application form for granting of medicine, medical devices and related products manufacturing license. Site plan has to be submitted in a form “Site Master File”. this may be applicable for Ayurvedic Manufacturing Unit, Homeopathic manufacturing unit, cosmetic manufacturing and Nutraceutical […]
Read MoreHow to start Factory in India?
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- by Ajay Kamboj
If you are going to start any Pharmaceutical, Ayurvedic, Cosmetic and Food & dietary supplements manufacturing unit and that requires more than ten workers then you have to register your manufacturing unit under Factory Act, 1948 also along with required licenses and documents required for starting pharmaceutical manufacturing unit, Ayurvedic Manufacturing Unit, Cosmetic Manufacturing Unit […]
Read MoreWHO Good manufacturing practices for pharmaceutical products
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- by Ajay Kamboj
GMP is that part of quality management which ensures that products are consistently produced and controlled according to the quality standards appropriate to their intended use and as required by the marketing authorization, clinical trial authorization or product specification. GMP is concerned with both production and QC. GMP is aimed primarily at managing and minimizing […]
Read MoreWhat is BIHRT? Is it legal to compound and manufacture BIHRT in India
- by Ajay Kamboj
What is BIHRT? Bioidentical Hormone Replacement Therapy. BIHRT is the use of supplemental doses of hormones that have a chemical structure identical to the hormones that the human body naturally produces. Query: I have a query regarding the regulatory requirements of compounding pharmacies in India. Do Bioidentical hormones come under the category of Ayurvedic […]
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