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Children’s Product Certificate (CPC) | CPSC.gov

Manufacturers and importers of children’s products must certify, in a written Children’s Product Certificate (CPC) based on test results from a CPSC-accepted laboratory, that their children’s products comply with applicable children’s product safety rules.The CPC and supporting test reports must be in English. The list of children’s product safety rules to consult and to cite in a ...

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REPS India

REPS India is a public register which recognises the qualification and expertise of exercise instructors. REPS mission is to work with the entire fitness industry to ensure that all exercise professionals are suitably knowledgeable and qualified to deliver safe and effective instruction, and to …

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As of 1st April 2018, there are 50 products that fall into the category of products that require Compulsory Registration. A. Who can Apply? Manufacturers of the products notified in the scheme which is located in India or outside India. The separate Registration number for products being manufactured at different locations.

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Diaper Raw Material Manufacturer | FibrilTex India Pvt. Ltd.

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FDA Registration Number - FDA Registration Certificate

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Format – Declaration to ensure a Supplier registered as ...

Feb 08, 2019·Let us help you to recall that the MCA has recently been issued one notification w.r.t. the specified Companies (Furnishing of information about the payment to Micro and Small enterprise suppliers) Order, 2019 on 22nd January 2019 (hereinafter referred to as “the Order”) to roll out a new e-form MSME FORM 1 and also to define the due dates by which need to be filed.

TENDER FOR SUPPLY OF ADULT DIAPER (LARGE SIZE) TO …

LIMITED TENDER NO.:- BPPI/LTD./SURGICAL-093/2019 TENDER FOR SUPPLY OF ADULT DIAPER (LARGE SIZE) TO Bureau of Pharma Public Sector Undertakings of India (BPPI) For the year 2019 BUREAU OF PHARMA PUBLIC SECTOR UNDERTAKINGS OF INDIA (Set up under the Department of Pharmaceuticals, Govt. of India) 8th Floor, Videocon Tower, Block E1,

India Office | FDA

Aug 03, 2020·Established in November 2008, the India Office serves as the lead FDA on-site presence in India. The mission of the New Delhi-based office is to help ensure the safety, quality, and effectiveness ...

Central Drugs Standard Control Organization

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Guidelines – NAFDAC

These guidelines are to enable applicants obtain detailed provisions of how to undertake their requested service from NAFDAC. The guidance documents are categorized based on product type and do provide detailed information on: Application, Facility Inspection, Documentation, Labelling, Tariff (Fees) and Timelines.

Clinical Research Regulation For India | ClinRegs

Clinical Trial Registration. Per the 2019-CTRules, the G-ICMR, and IND-31, it is mandatory for all sponsors (applicants) to register their clinical trials, including academic trials, with the Indian Council of Medical Research (ICMR) ’s Clinical Trials Registry - India (CTRI) ( IND-57) before initiating a study.

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Diaper - Manufacturers & Suppliers in India

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TENDER FOR SUPPLY OF ADULT DIAPER (EXTRA LARGE SIZE) …

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Product certification - Wikipedia

Product certification or product qualification is the process of certifying that a certain product has passed performance tests and quality assurance tests, and meets qualification criteria stipulated in contracts, regulations, or specifications (sometimes called "certification schemes" in the product certification industry).. Most product certification bodies (or product certifiers) are ...

India Drug Registration - Pharmaceutical Consulting

Obtaining approval for the import of drugs into India consists of up to three main phases: New drug approval – the product must go through an approval process to obtain a drug registration (this regulation is dependent upon the type of pharmaceutical and whether a predicate drug or substance is already marketed in India, is not necessarily only for new drugs, and must be received from the DCGI).

Mandatory requirements to get FSSAI License in India

Jan 16, 2020·FSSAI registration or License is mandatory for all types of food business operators in India whether they are transporters, distributors, manufacturers or caterers, etc. there are 3 types of registration available depending upon the annual turnover and type of the establishments or business.

Registration and Listing | FDA

The Voluntary Cosmetic Registration Program (VCRP) is an FDA post-market reporting system for use by manufacturers, packers, and distributors of cosmetic products that are in commercial ...

Home | Hindustan Unilever Limited website

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Home | Hindustan Unilever Limited website

Home | Hindustan Unilever Limited website. LATEST NEWS. HUL to become 100% plastic neutral by 2021. We continually look at new ways to reduce, re-use, recycle and recover packaging and waste as we move towards becoming a zero-waste business. Read more View all our news and features.

CDSCO Releases Frequently Asked Questions on Import and ...

Nov 07, 2019·Registration Certificate is a certificate issued under Rule 27A of Drugs and Cosmetics Rules, 1945 by the Licensing Authority in Form 41 for registration of premises and the drugs manufactured by the manufacturer meant for import into and use in India.

Permission And License Required To Make Cosmetics In India

Jun 09, 2017·Every cosmetic product got manufactured by the manufacturer for the import under the Registration Certificate into India must conform to the specifications and guidelines that are defined in the Drugs & Cosmetics Rules, 1945 as amended from time to time. The registration provided to the manufacturer is valid for a period of three years.

REX Certificate | Process flow of how to get a ...

The application for registration under REX certificate is required to be filled in the format 1C. The REX system in export has a pre-application part known as the AREX form. You can fill in your details in this form and take a printout. It has to be signed by the applicant and submitted to the Local User.