Indian Pharmacopoeia Commission Recruitment 2016

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Indian Pharmacopoeia Commission (IPC) has released Notification Regrading IPC Direct Recruitment 2016 . Indian Pharmacopoeia Commission (IPC) Has Invited Application Form For 16 Pharmacopoeia Scientists . All Eligible Candidates Are Required To check Eligibility details for IPC Job Advertisement and Apply Offline Before Or On 11-07-2016 (11th July 2016).he details of Indian Pharmacopoeia Commission latest jobs alert Employment News, Careers, Vacancy, Syllabus, Interview Date, Interview Time, Admit Card, call Letter, Result, Merit List, etc.., Get more updates from

Indian Pharmacopoeia Commission Direct Recruitment

No Of Posts : 16  
Direct Recruitment 
Name of Post : 
1. Senior Pharmacopoeia Scientists - 04
2. Pharmacopoeia Scientists - 12 posts

Qualification :  
 All Interested Candidates should have completed Post Graduation Degree, PhD. Degree or its equivalent qualification from a recognized Board/University. For Post Wise Qualification Details Go To Detailed Official Notification.

Also Read :   

Age Limit : 
For Postwise Age Details Go To Detailed Official Notification.

Pay Scale :
INR Rs. 1,00,000/- (Post 1), Rs. 50,000/- (Post 2).

Selection Process : 
Selection Process Details Go To Detailed Official Notification.

Also Read  : Interview Tips For Freshers/Exp 

Application Fee :
Application Fee Details Go To Detailed Official Notification.

How to Apply :  
All Eligible job seekers Can Download application Form through official website After Filling The application form, candidate must send hard copy of application along with relevant testimonials (Mentioned In Detailed Advertisement) to the following Address before or on 11-07-2016.

See More : Ghaziabad Jobs

Important Dates to Remember :
Last Date for Receiving of Application Form Is: 11-07-2016 . 
You may get other details about Indian Pharmacopoeia Commission Direct Recruitment 2016 through this Official Notification.Interested aspirants can stay connected with web portal to achieve latest updates for Indian Pharmacopoeia Commission. 

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About Indian Pharmacopoeia Commission
 Indian Pharmacopoeia Commission (IPC) is an Autonomous Institution of the Ministry of Health and Family Welfare, Govt. of India. IPC is created to set standards of drugs in the country. It’s basic function is to update regularly the standards of drugs commonly required for treatment of diseases prevailing in this region. It publishes official documents for improving Quality of Medicines by way of adding new and updating existing monographs in the form of Indian Pharmacopoeia (IP). It further promotes rational use of  generic medicines by publishing National Formulary of India.
IP prescribes standards for identity, purity and strength of drugs essentially required from health care perspective of human beings and animals.
 IPC also provides IP Reference Substances (IPRS) which act as a finger print for identification of an article under test and its purity as prescribed in IP.
 IP standards are authoritative in nature. They are enforced by the Regulatory authorities for quality control of medicines in India. During Quality Assurance and at the time of dispute in the court of law the IP standards are legally acceptable.
 IP is an official document meant for overall Quality Control and Assurance of Pharmaceutical products marketed in India by way of contributing on their safety, efficacy and affordability. The work of the IPC is performed in collaboration with members of the Scientific Body, subject experts as well as with representatives from Central Drugs Standard Control Organization (CDSCO), State Regulatory authorities, specialist from Industries, Associations, Councils and from other Scientific and Academic Institutions.
 IP contains a collection of authoritative procedures of analysis and specifications for Drugs. The IP, or any part of it, has got legal status under the Second Schedule of the Drugs & Cosmetics Act, 1940 and Rules 1945 there under.     
As per the policy of IPC, IP monographs are not framed to detect all possible impurities. The prescribed tests are designed to determine impurities on which attention are required to be focused, to fix the limits of those that  are tolerable to a certain extent, and to indicate methods for ensuring the absence of those, that are undesirable. It is, therefore, not to be presumed that the impurities can be tolerated because they have not been precluded by the prescribed tests.
Distinction exists between Pharmacopoeial Standards and Manufacturer’s release specifications. Pharmacopoeial standards are publicly-available compliance document that provide the means for an independent check about the quality of a product, all time during its shelf-life. To ensure compliance related to pharmacopoeial requirements, the manufacturer’s specifications may need to be more exacting than corresponding pharmacopoeial specifications.
The Govt. of India have created a separate, dedicated, autonomous institutionin the form of the Indian Pharmacopoeia Commission (IPC) to deal with matters relating to timely publication of the Indian Pharmacopoeia which is the official book of standards for drug included therein, in terms of the Second Schedule to the Drugs and Cosmetics Act, 1940 so as to specify the standards of identify, purity and strength of the drugs imported, manufactured for sale, stocked or exhibited for sale or distributed in India.
The mandate of the Commission is to perform, inter-alia, functions such as revision and publication of the Indian Pharmacopoeia and National formulary of India on a regular basis besides providing IP Reference Substances and training to the stakeholders on Pharmacopoeial issues. The Commission has become fully operational from 1st January, 2009 as an Autonomous Body, fully financed by the Central Government with specific budgetary allocations under administrative control of the Ministry of Health and Family Welfare. The Secretary, Ministry of Health and Family Welfare, is the Chairperson and the Chairman-Scientific Body is the Co-Chairman of the Commission. The Secretary-cum-Scientific Director is the Chief Scientific and Executive Officer of the Commission.
To promote the highest standards of drugs for use in human and animals within practical limits of the technologies available for manufacture and analysis
Develop comprehensive monographs for drugs to be included in the Indian Pharmacopoeia, including active pharmaceutical ingredients, pharmaceutical aids and dosage forms as well as medical devices, and to keep them updated by revision on a regular basis.
Develop monographs for herbal drugs, both raw drugs and extracts/formulations therefrom.
Accord priority to monographs of drugs included in the National Essential Medicines List and their dosage forms.
Take note of the different levels of sophistication in analytical testing/ instrumentation available while framing the monographs.
Accelerate the process of preparation, certification and distribution of IP Reference Substances, including the related substances, impurities and degradation products.
Collaborate with pharmacopoeial bodies like the Ph Eur, BP, USP, JP, ChP and WHO with a view to harmonizing with global standards.
Review existing monographs periodically with a view to deleting obsolete ones and amending those requiring upgrading /revision.
Organize educational programs and research activities for spreading and establishing awareness on the need and scope of quality standards for drugs and related articles /materials.
Publish the National Formulary of India for updating medical practitioners and health professionals.
Indian Pharmacopoeia Commission Recruitment 2016 Indian Pharmacopoeia Commission Recruitment 2016 Reviewed by Ramesh Reddy on 21:59:00 Rating: 5
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