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Validating Software as a Medical Device (SaMD)
FDA Form 483. The term “Form 483” is enough to make anyone in the medical device industry shudder. FDA inspections are stressful, but receiving a …
Food firm in China and two US companies warned about violations
… Code of Federal Regulations, part 117 (21 CFR part 117) and resulted in the issuance of an FDA Form 483. The significant violations are…
Marvel Biosciences Corp. to Commence cGMP Manufacturing of Its Lead Asset MB-204
An US-FDA Form 483 is issued to management at the conclusion of an US-FDA inspection when an investigator(s) has observed any conditions that in …
Common GCP Bioresearch Monitoring Violations
After an inspection, FDA investigators may issue a Form 483 to communicate any onsite findings of noncompliance with FDA’s regulations. BIMO also …
ADMA Biologics Announces Successful Completion of FDA Pre-Approval Manufacturing Facility …
The PAI successfully concluded with the FDA issuing zero Form 483 observations in the Agency’s determination that the Company’s Boca Raton, …
FDA Releases Guidance On CMC Changes To An Approved Application: Certain Biological Products
… he assists companies by providing internal and external audit support as well as FDA 483 and warning letter response and remediation services.
Computer System Validation Boot Camp : A 5 Day Complete Immersion in the Validation Process …
Agenda Highlights Module 1: FDA Compliance (CSV regulations; compliance toolset; Form 483 ; ICH/ PICS guidelines; Eudralex Annex 11, 20, and III).
FDA slams unapproved flu vaccine seller Davati Medical
Offering the sale of unapproved influenza vaccine Fluzalp Quadrivalent has landed Davati Medical Supply with a US FDA warning letter.
EAS Consulting Group Collaborates with Food Safety Foundation for Innovative Approach to Food …
… or support after receipt of a FDA form 483 or Warning Letter, including market withdrawals, recalls and improvement plans with follow-on mock-FDA …
Computer System Validation Online Professional Certificate Program, August 23rd-27th, 2021 …
… FDA Form 483; FDA Warning Letter; FDASIA; Eudralex Annex 11, 20, and III; ICH Guidelines; PIC/S Guides; Exercise: Exploring the regulations …

Brazil coronavirus deaths climb to 46,510, cases near 1 million
By Admin
Brazil recorded 1,269 additional COVID-19 deaths on Wednesday, bringing its official death toll from the novel coronavirus to 46,510, the most in the world outside...
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Requiring masks ‘political hazard’ as COVID-19 surges in California breadbasket
By Admin
The first wave of COVID-19 came slowly to San Joaquin County in the heart of California's breadbasket, but the much-feared second surge is roaring through,...
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Mothers as ‘trauma surgeons:’ the anguish of raising black boys in America
By Admin
Raising black boys in America involves "constant mental anguish," Danielle Pattillo, a special education teacher in New York City and mother to two sons, ages...
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Record spike in new coronavirus cases reported in six U.S. states as reopening accelerates
By Admin
New coronavirus infections hit record highs in six U.S. states on Tuesday, marking a rising tide of cases for a second consecutive week as most...
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Some Amazon villagers eschew drugs for COVID-19, take ‘toothache plant’ herbal tea
By Admin
Some villagers in the eastern Amazon are spurning Brazilian government advice to take the malaria drug hydroxychloroquine to keep the novel coronavirus at bay and...
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Pharmacognosy

By Admin on September 5, 2019

History. Defination and Scope of Pharmacognosy. Drugs and Pharmaceuticals. Aids of natural origin. Classification of Natural Drug. Introduction to part of a plant. Scheme of Pharmacognostic Studies. Collection and Preparation of Natural Drugs for Market. Adulteration. Drug Evaluation and significance of pharmacopoeial Standards. Chemical Nature Drugs. Surgical Fibres. Sutures and Dressings. Taxonomical classification of Curde Drugs. Biological Name of Natural Drugs .

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Also Read: The Pearson Guide to GPAT & Other Entrance Examination in Pharmacy 2019 (Jan 2018 Paper Included)

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