29 November 2010

Organ donations in India can get a new life through better laws


Inadequate laws for organ donation in India and lack of knowledge about what to do to donate one’s body parts after death, keep even supportive people from making a legally binding commitment.
For instance, few people know that they can mention it in their wills that their body parts such as kidneys, liver and eyes should be donated after death.
Experts say making it mandatory for all people to express a choice in the matter of organ donation, would increase donations and go a long way towards meeting the shortage of organs for transplant.
With the world celebrating the Sixth (India’s first) International Organ Donation Day on November 28, it may be educative to examine what other countries have done to promote organ donation.
Many countries have adopted a ‘presumed consent’ policy and have passed laws for its implementation. Under this policy, the state presumes that a deceased citizen has said yes to organ donation, unless he has opted out by mentioning this in a legally accepted document.
Dr Sunil Shroff, head of the department of urology and renal transplantation at Sri Ramachandra Medical College and Research Institute in Chennai, said that under ‘presumed consent’ law, the consent of family members is not required. In the event of a person’s death, his/her organs can be retrieved without delay.
The ‘presumed consent’ law was first passed in 1989 by Spain which, till then, had one of the lowest organ donation rates in the world. But thanks to the law, it now has the best organ procurement programme in the world.
Today, Spain has 34 per million person donation rate, despite the fact that it has one of the lowest incidence of road mishaps in the European Union. In contrast, India has just 0.1 per million person donation rate.
The ‘presumed consent’ law now exists in Belgium, Austria, Finland, France, Norway, Spain and Singapore and UK, too, may pass the law soon. Dr HL Trivedi of the Institute of Kidney Disease and Research Centre (IKDRC), Ahmedabad, said the law had led to a dramatic increase in donations in these countries.
"The law has, to a large extent, helped these nations overcome their shortage of organs for donation," Trivedi said.
Dr Shroff, however, said that legislation of a 'presumed consent' law is unlikely to be accepted in India "India has not yet reached that level of awareness that makes organ donation from cadavers a routine matter," he said. "Hence such a law would not help us."
Some other countries, however, have made it mandatory for their citizens to make a choice whether or not they wanted their organs to be donated.
The 'mandatory choice' legislation has been in place in Sweden and Denmark since 1996. Because of this law, Sweden's potential national donor registry has swelled by 6 lakh and Denmark's has increased by 1.5 lakh.
Medical experts are of the view that India, too, should make it mandatory for citizens to declare their choice regarding donation of their organs for transplantation. This can be done by registering with a national body or expressing a choice during issue of important documents such as driving license or national identity card or passport, experts said.
They, however, added that even for 'mandatory declaration' to succeed, there is an urgent need to raise the level of awareness of organ donation in this country.

25 November 2010

openings with Ascenders for SAS programmer

Summary
Experience: 2 - 3 Years
Location:Bengaluru/Bangalore
Compensation:Rupees 4,00,000 - 5,00,000
Education:UG - Any Graduate - Any Specialization
PG - Post Graduation Not Required
Industry Type:Pharma/ Biotech/Clinical Research
Role:Clinical Research Associate/Scientist
Functional Area:Healthcare, Medical, R&D
Posted Date:25 Nov
Desired Candidate Profile
• Has basic understanding of Statistical principles and can understand with some guidance the statistical analysis principles of the SAP.
• Has good understanding of 21 CFR-Part 11 and GCP and GPP principles.
Job Description
• At least 2-3 years SAS programming experience in the Clinical Domain
• Can write programs related to Clinical Trial Analysis as per SAP independently or with very little guidance ( Derived Dataset Programming, TFL programming)
Keywords: sas programmer
Company Profile
-
Contact Details
Company Name:Ascenders
Website:Not Mentioned
Executive Name:Naina Khade
Address:Not Mentioned
Email Address:jobs@ascenders.co.in
Telephone:022-25623134

opening for Sr. SAS programmer @ Banglore

Summary
Experience: 4 - 6 Years
Location:Bengaluru/Bangalore
Compensation:Rupees 5,00,000 - 8,00,000
Education:UG - Any Graduate - Any Specialization
PG - Post Graduation Not Required
Industry Type:Pharma/ Biotech/Clinical Research
Role:Clinical Research Associate/Scientist
Functional Area:Healthcare, Medical, R&D
Posted Date:25 Nov
Desired Candidate Profile
• Has moderate level understanding of Statistical principles and can understand with little guidance the statistical analysis principles of the SAP.
good understanding of 21 CFR-Part 11 and GCP and GPP principles
• Has good
Job Description
• At least 4-5 years SAS programming experience in the Clinical Domain
• Can write programs related to Clinical Trial Analysis as per SAP independently ( Derived Dataset Programming, TFL programming, Exploratory Analysis Programming)
Keywords: sas programmer
Company Profile
-
Contact Details
Company Name:Ascenders
Website:Not Mentioned
Executive Name:Naina Khade
Address:Not Mentioned
Email Address:jobs@ascenders.co.in
Telephone:022-25623134

Opening with Icon for SAS programmer

Looking for an experienced SAS Programmer/ SAS Lead with good knowledge
B.Sc (Masters Preferred ) in one of the following fields: Computer Science, Statistics, Mathematics, or relevant science with experience in the Pharmaceutical Industry.
Qualifications:
At least 0- 2 years experience of processing clinical trial data using SAS. At least 0- 2 years of management experience preferably associated within a programming environment and/or with formal drug submissions to regulatory agencies
Sound knowledge of computer hardware, software, and data processing techniques.
Strong skills in project management including time management, planning, problem solving, ability to interface with all levels and different cultures, both internally and externally are required.

Required skills include:
Proficient programming skills in SAS; Sound knowledge of the Software Development Life Cycle and its application in a R D environment; Ability to critically review data; Good oral and written communication skills; Good interpersonal skills and team player.

Kindly revert back with the following details.
Current CTC, Expected CTC, Total Experience, Notice Period.

Neil
Nilamadhab.Mahapatra@iconplc.com
044 4390 2958
ICON Clinical Research India Pvt Ltd
Url: www.iconclinical.com

opening with Tata Consultancy Services for Clinical Data Management.

This is for a Team Lead position.

Candidates need to be flexible with any shift incl night shifts.

 Academic Qualification :

o Graduate/Postgraduate in Science

Experience:

o Minimum 4 years experience with 2+ years in CDM with atleast 6 months in leading a project
o Solid experience and understanding of ICH GCP principles, clinical drug development process, organizational, communication and data management skills

 Others:

o Capability to lead by motivation and example
o Ability to prioritize schedule and organize
o Knowledge of Oracle, PL/SQL is required.
o Knowledge of SAS is required.
o Excellent interpersonal and communication skills
o General knowledge of Clinical Trials and Pharmaceutical Industry

If interested revert asap.

Sharon
Recruitment Officer
Tel : 022-65904515
sharon@globalsearchservices.com
GlobalSearch Services
101,Shubam Palace, Sector 15, Kopar Khairne,Navi Mumbai - 400709

Sibutramine- an Anti-obese drug suspended by DCGI

The Drugs Controller General of India (DCGI) on Friday ordered the “suspension” of the manufacture and import of anti-obesity drug Sibutramine after the medicine showed serious side effects, including heart attack, among some users. The DCGI also recommended to the Ministry of Health and Family Welfare a total ban on the sale of the drug.

It proposes the setting up of various committees to oversee the safety of drugs and also the feasibility of introducing new drugs in India.

The suspension order was issued under Section 26 (A) of Drugs and Cosmetic Act, with immediate effect, with the DCGI also seeking a total prohibition on its manufacture and sale in the open market. The ban has to be formally notified by the Health Ministry on the recommendation of the DCGI.

The decision was taken following recommendations of an expert committee comprising pharmacologist Y.K. Gupta (All-India Institute of Medical Sciences), endocrinologist A.C. Ammini (AIIMS) and S.D. Seth (Institute of Clinical Research) and Anoop Misra (Fortis Hospital).

Orlistate is now the only drug in the market for obesity-management and weight loss, though many new drugs are expected to be in the market shortly.

The decision to ban Sibutramine, sold under different brand names, was taken after studies found it increased the risk of heart attack, stroke and death. The drug has already been banned in the United States, Canada and Australia and was withdrawn in China on Tuesday. The European Medicine Agency (EMA) too has recommended complete withdrawal of this drug.

The preliminary reports of the “scout trials” on Sibutramine showed increase in heart rate and blood pressure among users. This was further confirmed in the final finding of the trial, promoting the government to take prohibitory action.

This is the third drug relating to diabetes and obesity that has been banned in India in the last one-and-half years.

Last month, the government banned the import and manufacture Rosiglitazone, an anti-diabetic drug. Rosiglitazone is already banned in Europe after users experienced serious side effects, including cardiovascular events and adverse effects on lipid profile.

Prior to that, anti-obesity pill Rimonabant was banned in March 2009 after it was found to cause depression and suicidal tendencies.

One of the most commonly prescribed medicines for weight loss and obesity management, Sibutramine has been available in India since 1999. It is manufactured and marketed by over 20 generic companies under various brand names.

22 November 2010

Sr. Product Development Manager - Food / For Bira Life Sciences/ Mumba

Sr. Product Development Manager - Food / For Bira Life Sciences/ Mumba
Posted by: BIrla Life Sciences - A Yash Birla Group
Posted date: 18-Nov
Job Description:Bench top/ Pilot Plant development/ Formulation of Food Products Prdct Testing/ Shelf Life testing. Scale up &Commercialization of prdts developed 3rd party vendor Sensory Evaluation/ Ingredient sourcing/development of the new products.PFA Foods App

Desired Candidate ProfileFood formulation/culinary ability/Food Testing skills- chemical, physical and analytical/ PFA Foods Knowledge/Sensory Evaluation/ Knowledge of food manufacturing processes, GMP s HACCP. Prdt R&D from concept to finished product (commercial).

Experience Required: 8 - 12 Years

Education Required: UG - Any Graduate - Any Specialization PG - Any PG Course - Any Specialization
More....http://www.spanjobs.com/india/jobs/retail-merchandising-jobs/mumbai-jobs/sr-product-development-manager-food-for-bira-life-sciences-mumba/1402663?action=search&offset=585&utm_source=Indeed&utm_medium=organic&utm_campaign=Indeed

18 November 2010

Bio Pharma Industry Associate Job - ScienceCentre.in

Science Centre has been set up by the Clinnovo Research Labs, Hyderabad, as its subsidiary with the aim of bridging the gap between the biomedical sciences education and professional career in industry and academic centers of excellence.


Science Centre announces BIOPHARMA INDUSTRY ASSOCIATE positions for entry level and senior professionals in the clinical/biopharmaceutical arena.


The one year associate position will involve training from experts and working as associates in ongoing clinical,imaging and informatic projects. At the end of one year candidates will have the possibility of continue their positions at Science Centre, subject to their work performance during the one year period.


Associates will be rotated among different departments and will work on projects involving international collaborations and MNC sponsors.

For More check
http://sciencecentre.in/?cont=industry-associate