dear admin;
i hav received email from you, informing me my marks . thanks for sending me email. but, when can i expect original certificate.
dr.r.srinivasa rao
S07 PRAF10094
industrail programme in pharma regulatory affairs

Sneha Diagnostics launches India's first Medical Diagnostics Blog

Sneha Diagnostics , the fastest growing medical diagnostic services provider in India, launches India's first Medical Diagnostics Blog http://www.diagnosticsblog.com

This blog brings you in a single location many useful Articles, news, trends, profiles and innovations in Medical Diagnostics (Radiology, Pathology, Clinical Laboratory), Preventive health care, Rural health care, Medical Tourism and other health care related areas (mainly from India ).

Since it's beta launch in December 2007, it has been attracting thousands of visitors across the globe who want to know more information in the above health related fields in India.

If you like to publish any diagnostics related articles /news, please send us: publish@diagnosticsblog.com


Sneha Diagnsotics

Prakasam Road, Near I.V.Palace
Governorpet, Vijayawada, AP, India
Tel: 91-866-244 1012 /244 1022
Fax: 91-866-244 1020

For more information about this blog, please send an email: info@diagnosticsblog.com

Visit http://www.snehadiagnostics.com to learn more about Sneha Diagnostics.

Global Conference on Clinical Research and Drug Development

Institute of Clinical Research (India) is organizing 5th Global Conference on Clinical Research and Drug Development. Following are the details about the conference:

Sponsored by : Department of Science and Technology, Government of India
Venue : Hotel Intercontinental The Grand, Mumbai
Dates: : October 10th & 11th, 2008


Contact for Registration:
Mr.Sameer Gupta, National Manager
Mobile no: +91- 9324610056
Email: sameergupta@icriindia.com


The conference will focus on recent advances and business opportunities in Clinical Research. About 400 delegates are expected to participate in the two-day event. The unique feature of this conference is that 10 International keynote speakers from US, Canada and UK along with highly acclaimed and eminent speakers of India from various Pharmaceutical Companies, CROs and Regulatory Bodies would be sharing their views and opinion in the conclave. The conference is designed for expert level professionals in the Pharmaceutical, Biotechnology, Medical Devices, Government, Support Services/Products, Academia, Logistics, Venture Capitalists, Bank, Insurance and related Healthcare Industries.

The conference could be attended by individuals involved in:
• Clinical Research and Development
• Clinical Safety and Pharmacovigilance
• Clinical Supply Operations
• Clinical Trial and Project Management
• Data Management
• Drug Development and Discovery
• Investigator Site Management
• Medical and Scientific Affairs
• Academia
• Outsourcing Management
• Contract Research Organizations
• Post-graduate Students Entering Pharmaceutical Industry
• Procurement and Purchasing
• Quality Assurance
• Regulatory Affairs
• Government and Public Policy; Lawmakers
• Senior and Executive-Level Decision Making for Clinical Trial

Regulatory Professionals :Goals and Roles

· Regulatory Affair Associate:
This profile is more about providing consultancy,where a person can play a lead role as a decision making considering all pros and cons.This type of role will suit people who enjoys taking tasks as a challenge, want additional responsibility, and enjoy the buzz and pressure of a dynamic environment.


Regulatory Affairs Assistants:
Providing administrative Regulatory support for timely delivery of products by assisting with technical support.
Prepration and submission of design dossier with approval body
Preprations for FDA and notified body inspection.
Assembly and submission of design dossier and technical document.


Quality Assurance Associate:
Again Pharmaceutical Quality Assurance professionals work as consultants

To provide audit and quality assurance services to ensure product success.
They play a vital role in developing pharmaceutical products that protect patient safety and ensure regulatory compliance.
By employing their vast skills and resources, professionals with their experience and knowledge to save money, minimize your risk and facilitate your project speed.

Quality Assurance Investigators

§ Professionals possess thorough knowledge of GMP / GLP regulations like US FDA, WHO GMP, ICH, MHRA, ANVISA, requirements of cGMP documents (SOP's/ Change controls/ Deviations) as per various regulatory agencies.

§ Professional supports other member of regulatory teams in review and filing of various dossiers in US/EUROPE/CANADA/MCC/BRAZIL and various regulatory agencies across the globe.

§ Professionals Implements higher standard of quality in all areas of ANDA submissions for Tablets / Capsules /Dry Syrups/Oral solutions.

§ Professional assists in preparation of supplements, annual reports and amendments,Review of Stability data/Trends/Impurity profiles and perform various regulatory inspection.

• 
  Documentation Administrators
  Plan and organize internal and external meetings and teleconferences.
  Liaise with CROs, clinical sites, Clinical Investigators and others, as required
  Maintain paper-based and electronic files for Clinical and Regulatory departments
  Ability to develop and maintain indexing and filing system for Clinical and Regulatory documentation in line with regulatory requirements
  Receive, identify and file documentation in accordance with filing system.
  Generate listings of documents received and filed.
  
  Medical Information Associate:
  
  Professionals will be involved in setting up new global processes and systems to align all affiliates & distributors for medical information.
  
  Professionals act as the key point of contact for medical information enquiries locally & from international affiliates.
  
  Professionals are Responsible for composing written & verbal responses to internal and external customers.
  
  They are also responsible Literature searches & literature reviews and updating medical information database.
  
  
  
  
  
  
  

Job opportunities at Sneha Diagnostics

Please visit our career link: http://www.snehadiagnostics.com/existingopenings for various openings

Please send your resume to : hr@snehadiagnsotics.com

Source:The Economic Times

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Source:The Economic Times

Sneha Diagnostics will soon open world class medical diagnostic center in Vijayawada, AP, India

Sneha Diagnostics will be soon opening a new world class medical diagnostics centre in Vijayawada,AP,India.

We're looking for well experienced medical consultants (all specializations ) to join full-time /part-time (flexible hours ) basis at our Vijayawada centre.

Please send your detailed resume to : hr@snehadiagnostics.com

Sneha Diagnostics

Prakasam Road, Near I.V.Palace
Governorpet, Vijayawada, AP, India

Tel: 91-866-244 1012 /244 1022
Fax: 91-866-244 1020

Email: vja@snehadiagnostics.com

http://www.snehadiagnostics.com/

Presentation On CV Making

Source:HT,Wednesday,september 10,2008

Source: HT,Wednesday,September 10,2008

Regulatory Affairs :Future Of Professionals

As Pharmaceutical Industry is confronting a stiff competition and escalating towards growth and the same sector is experiencing growth opppurtunities. As society is maturing,more attention is being paid to the areas relating to new drug development and health care improvements so that the end users can get quality health care services.

As mentioned earlier not only pharmaceuticals but medical device and biotechnology industry are experiencing invariable growth stimulated by growing market opportunities and advancement in the field of biology and technology .Development of new therapeutics and diagnostics consequently creating tremendous job opportunities in regulatory and clinical research sector.

Biopharmaceutical industry is facing increase in demand in terms of quality of research and development consequently experiencing a positive impact on job market.This sector is currently seeing shortage of well versed and skilled professionals and moreover professionals are entering indirectly in this sector.By and large professionals learn more about requirements from their partners,various publications,latest developments and amendments in the regulatory sector.

Again experience matters a lot relative to academic qualification, this is due to the fact that professionals who are working in professional environment and students who have just completed their academic qualification and want to switch over to job can bring in the discontinuity in between completing academic qualification and searching for a regular employement.

Current regulatory affairs professionals are keen to prepare regulatory affairs professional by volunteering and highlighting the challenges and upcoming opportunities for their colleagues with in their organization and imparting academic and professional knowledge for becoming next generation regulatory affair professional

Tripping Into Regulatory Affairs...and Glad to Be Here

Preventive Healthcare Seminar organized at BII Noida

A seminar on “Preventive Healthcare” was organized at BII Noida on 4th sept’08 by Kailash Hospital. The seminar was attended by the Program Director, faculty, students & other staff members of BII

















Mr.Sankalp Bansal, Chief Operating Officer from Kailash Healthcare Ltd provided with some vital information on:

• Rising health issues in India
• Importance of regular health check ups and
• Key preventions one should take up in order to live a healthy, disease-free life.


The seminar was quite informative and was appreciated by one and all.

10 Facts: Why I Want to Become Regulatory Affairs Professional

I. Most rewarding,future secured,challenging and one of the highly paying career in its class.

II. Most interesting and employee friendly environment in companies to work for.

III. Tremendous job opportunities are created day by day in this particular sector.

IV. Relatively Excellent opportunities for those with medical and life sciences background.

V. Professionals drawing handsome salaries as compared to their peers in other areas of pharmaceutical and biotechnological industry.

VI. Many countries still facing dearth of regulatory affairs professional including India and Japan. SOURCE:http://www.heidrick.com.

VII. Professionals with Regulatory affairs certification had an edge over others and moreover these professionals are preferred while hiring.

VIII. Jobs and nature of work employed in this sector is considered as respectable.

IX. Professionals working as regulatory trainee can get frequent promotions definitely based on their performance as compared to their counterparts in various sectors.

X. Working professionals can easily get into this profession by simply joining a Distance Participation Progame In Pharma Regulatory Affairs.