Multinationals Geared Up Hiring For Regulatory Professionals

Many MNCs are on a hiring spree and are busy absorbing students for regulatory departments for CROs. Various international MNCs are cutting down their operations in foreign countries and expanding their business and workforce in India and moreover for their Indian operations they are endlessly recruiting for data management and regulatory affairs

Long considered a hub for regulatory clinical research by pharma multinationals because of quality,cost effective,English speaking workforce.Western countries which are majorly effected by the global meltdown has forced many MNCs to shut their shops in foreign countries and looking forward towards India as a place for opportunities .Along with multinational,many pharma majors and IT majors are also hiring.Stastics shows that India is the most favourable country.Recently India is leading to become most powerful and popular destination for regulatory clinical trials

In India not only clinical research but regulatory related clinical profiles is driving the employement sector. While drug majors are looking for the capable workforce,who can easily handle clinical data management and regulatory documents,which is quite a detailed procedures and moreover forms a part of research. Life sciences graduates are the most appropriate who understands glossary unlike in IT and banking.

National Bureau Of Agriculturally Important Microorganisms

Source :The Times Of India

Pharma Regulation & Clinical Trials Approvals Going e-governance

The concept of e-governance will likely to be launched and making the whole process quicker and simpler for pharma regulations and clinical trial approvals.













Source :The Economic Times

Bioinformatics Services

Inviting Tenders For Providing services For Bioinformatics Including Whole genome buffalo sequence SNP detection.

Source :The Times Of India

dear admin;

i have cleared all papers in APRIL 2008 for industrial programme in pharma regulatory affairs. i mailed you twice for original certficates. till now i didnt get them. pl do the needful and send me originals as i am leaving india shortly.

with regards

ramaraju srinivasarao

S07PRAF10094

BII active participation in Pharma Expo 2008

Bioinformatics Institute of India (BII) actively participated in 60th Indian Pharmaceutical Congress 2008 held at Netaji Subhas Institute of Technology, New Delhi from December 12 – 14, 2008.
The event was one of the largest events of pharmaceutical industry in India where more than 250 exhibitors took this opportunity to display their products & services. The event was attended by more than 8000 delegates including CEO’s , top executives of the pharmaceutical industry, R&D personnel, top officials of state & central agencies, academicians and teachers from medical and pharmacy colleges. There were huge networking & business opportunities for both exhibitors and delegates.

Bioinformatics Institute of India participated in the event with the objectives of creating awareness about various programs, trainings & services offered by the institution, to
interact with the medical and pharmacy students & to discuss business opportunities with Corporates. Mr. Vijay Shukla, Director BII and Dr. Kumud Sarin, Sr. Program Director BII were also present in the event BII along with the marketing and technical department of institution. All of them interacted very well with the students and officials from corporate to discuss the various training programs and services that can be taken up for the knowledge enhancement in the area of Bioinformatics, Pharma regulatory, clinical trials etc.

The event thus was quite successful and BII is looking forward to participate in much more events to follow in the pharmaceutical industry.

To view various programs & services offered by BII visit www.bii.in

For further details contact:
Bioinformatics Institute of India
C-56 A / 28, Sec – 62
Noida – 201301
U.P, India
Tel: 0120-4320801/02
9818473366, 9810535368
e-mail: info@bii.in
Web: www.bii.in

BII Active participation in Pharma Expo 2008

Bioinformatics Institute of India is actively participating in Pharma Expo 2008 which is going to held at Netaji Subhas Institute of Technology, Dwarka, New Delhi from December 12 – 14 2008.

The event is focussed on the pharmaceutical industry; more than 8000 delegates will attend the expo where 250 exhibitors are displaying their product & services.

The institute will take up this opportunity to display the various programs, trainings & services offered by them in the area of Bioinformatics, Pharma Regulatory, Clinical Trials etc.


To view various programs, training & services offered by BII visit: www.bii.in

Contact Bioinformatics Institute of India
Email: info@bii.in
Call: 9810535368, 9818473366

regarding assignments.............

thank you mam, for confirming about my asiignments..........

Indian Biotechnology Sector Is Thriving

Centralized Biotechnology Information System(BTISnet) is etablished by Govt. of India and inviting applications for Traineeship/Studentship in Bioinformatics

Source : The Times Of India

regarding the dispatch of assignments and research study

respected admin.
i am pursuing IIPR(Spring 2008)and my enrollment no. is S08IPPR10001.I had dispatched my assignments and research study to be eligible for the April 09 exams..................i just want to confirm whether it had reached u or not???????????kindly confirm it...i will be ever obliged for this!!!!!!!!!

Stringent Regulatory Norms For Medical Device Approval

The Indian Government may soon make it mandatory for medical devices such as stents,catheters,orthopedic implants and heart valves to obtain quality certifications before they reaches Indian medical device market.Products from both domestic and multinational medica device manufacturers must pass quality tests from standardizing bodies such as Bureau Of Indian Standards (BIS) or global quality solution provider Intertek

Leading players of medical device manufacturers such as siemens,Philips,GE and LG.India has a $2 billion medical device industry.The health ministry has asked Drug Controller General Of India (DCGI) to check marketing of forged and poor quality products.”The regulatory guidelines are ready and will be summitted it to the DTAB by the end of December for approvals.These guidelines would cover the definition,classification,certification and quality standards of medical devices.Whereas the standards are meant to test and verify medical devices,the classification will be in terms of risk associated with these devices.

The notified agencies would certify medical devices after auditing the quality,infrastructure,manpower and manufacturing plants of the company.The idea thus conceived to ensure access to safe,effective and clinically beneficial medical technologies for patients across the country

Certain medical devices are as important as life saving drugs;”There are devices which are implanted into human body for critical care.If not regulated patients may fall victim to poor quality medical devices.

Contact Information :DBT,Ministry Of Science And Biotechnology

E-mail address : swarup@dbt.nic.in

Website : www.dbtindia.nic.in

Source : The Economic Times

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