(Medical Devices Division)

Annexure-1 GMP CHECKLIST

SOP No.: EP-INS-004 Page 1 Annexure-1 GMP CHECKLIST (Based on WHO Good Manufacturing Practices (GMP) for active pharmaceutical ingredients stated as per

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INVESTIGATIONAL MEDICINAL PRODUCT …

C:\Users\website\Desktop\pendency july\IMPD Template Quality.doc Last printed 8/18/2016 8:02:00 PM INVESTIGATIONAL MEDICINAL PRODUCT DOSSIER FOR

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LIST OF NEW DRUGS APPROVED IN INDIA FROM …

LIST OF NEW DRUGS APPROVED IN INDIA FROM 1991 TO 2000 S. No Name of Drug Pharmacological action/ Indication Date of Approval 1 Ciprofloxacin 0.3% w/v Eye

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List of NABL Accredited Laboratories in India

Sr. No. Name of the Laboratory Nature of Lab Field Discipline Group Address Contact Details Organization Type 1 Alcatec Research Laboratories India Pvt.

(Medical Devices Division) - Central Drugs …

GUIDANCE DOCUMENT ON COMMON SUBMISSION FORMAT FOR IMPORT LICENSE OF NOTIFIED MEDICAL DEVICES. Page | 1 Guidance Document (Medical Devices Division)

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(Medical Devices and Diagnostic Division)

Central Drugs Standard Control Organization Directorate General of Health Services, Ministry of Health and Family Welfare, Government of India

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Manufacturing and Marketing permission issued …

S.No. Drug Name Indication Date of Approval 10 Everolimus tablets 2.5mg. 5mg and 10mg “Treatments of adults patients with progressive, well differentiated, non- ...

  Manufacturing, Marketing, Issued, Permission, Manufacturing and marketing permission issued

LIST OF LICENSED BLOOD BANKS IN INDIA * …

LIST OF LICENSED BLOOD BANKS IN INDIA * (February, 2015) Sr. No. State Total No. of Blood Banks 1. Andaman and Nicobar Islands 03 2. Andhra Pradesh 140 3.

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SUMMARY OF PRODUCT CHARACTERISTICS

Summary of Product Characteristics lactating women may be considered after careful evaluation of the benefits and risks in case of a medical emergency or an epidemic.

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GUIDELINES ON RECALL AND RAPID ALERT SYSTEM …

Page 3 of 13 5.0 Recall Classification: Recall classification is a numerical designation, I, II, or III, that is assigned to a particular product recall that indicates the relative degree of health hazard by country

  Recall

AORN Guidance Statement: Reuse of Single-Use Devices

program costs, including quality system require-ments such as sterility and post-processing device testing (see section on quality system require-

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GHTF SG3 Quality Management System - Medical Devices ...

Guidance on the control of products and services obtained from suppliers. GHTF/SG3/N17R9:2008 December 11, 2008 Page 7 of 21 Hardware is generally tangible and its amount is a countable characteristic (3.5.1). Processed

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Coding Guidance for Rotator Cuff Surgical Repair

Rotator Cuff Repair Clinical Documentation Guidelines Supporting Documentation: History and Physical: A full history and physical should be obtained from the referring physician detailing the signs, symptoms and conditions that deem the rotator cuff repair necessary.

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