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Clinical courses

 

Clinical courses

Pharma jobs, pharmaceutical jobs and recruitment for B.Pharm, M.Pharm in Baddi, Himachal Pradesh. Career for Pharmacists in Baddi. Freshers pharmacy recruitment in Baddi; Job for pharm.D, M.sc, m.pharm in faculty of pharmaceutics, pharmacology, pharmaceutical analysis, chemistry and jobs in pharmaceutical industry

  • Career for M.Sc./ B.Pharma as Executive/Jr. Executive – IPQA, QA (Oncology) in Panacea Biotec

    Panacea Biotec is a leading research based Health Management Company, with an annual turnover of approx. Rs. 830 Crores. We are engaged in research, development, manufacture & marketing of Vaccines, Bio-Pharmaceuticals and Pharmaceuticals (Rx & OTC) of international quality and Health Services. All Panacea Biotec plants are accredited by international agencies and they follow current Good Manufacturing Practices, as per WHO guidelines.
    We offer stimulating work environment & a career that spells growth. In tune with our plans, we require young, aggressive, dynamic, high performing and result oriented professional.

    Post: Executive/Jr. Executive – IPQA, QA (Oncology)

  • Enrolment Closing for the Professional Training Programs in Clinical Research and Pharmacovigilance (via Distance Learning) at Catalyst Clinical Services Pvt. Ltd.

    The enrolment for the Feb’14 batch of Professional Diploma in Clinical Research (PDCR) and Professional Certificate in Pharmacovigilance (PCPV) program is closing on 10-Feb-2014.Please send your Application Form by the due date in order to secure enrolment in Feb’14 batch

    These training programs are aimed at imparting knowledge and skills required for clinical research and pharmacovigilance profession thereby enabling the participants to explore a career in these emerging streams. Optimal course fee and ease of training and evaluation has led to the wider acceptability of the programs amongst students and researchers.

    Program(s) Highlights   Clinical Research and PV Opportunities
    • Optimal Duration : 6 months correspondence program, requires approximately 80 hours of total reading.
    • Assignment based evaluation, no written examination.
    • Optimal Course Fee.
    • Comprise of high quality study modules in line with the requirements of the clinical research and PV Industry.
    • Wide recognition and acceptance of the program through out the industry making PDCR India's largest CR training program.
    • Placement guidance provided to successful participants.
      • Global Clinical Research (CR) industry is estimated at $52 bn ofwhich CRO marketsize is estimated at$17.8 bn.
    • More than 2600 clinical trials are being conducted in India across 5000+investigator sites (ctri.nic.in)
    • The Pharmacovigilance (PV) market worldwide was $1860 million in 2008 & is estimated to reach $2252 million by 2015.
    • India is the fourth largest producer of pharmaceuticals in the world with more than 6,000 licensed drug manufacturers and over 60,000 branded formulations.
    • In India more than 150 companies are actively engaged in Clinical Research and Pharmacovigilance field.

     

    Professional Diploma in Clinical Research (PDCR)
    Module 1: Introduction to Pharmaceutical Medicine
    - New Drug Discovery
    - Clinical Development of Drug
    - Essential Clinical Trial Documents etc.
    Module 2: Good Clinical Practice (GCP) Foundations
    - History of GCP - milestones in the evolution of GCP
    - Principles of GCP
    - Ethics in Clinical Research
    - Biostatistics etc.
    Module 3: Drug Regulatory Affairs (Clinical Trials)
    - Overview of Regulatory Environment in USA, Australia, Europe & India
    - Clinical Trial Application Requirements in India
    - HIPAA Privacy Rule
    - IND/ANDA/New Drug Application etc.
    Module 4: Roles & Responsibilities of Clinical Trial Personnel

    READ MORE >>>

     

    Professional Certificate in Pharmacovigilance (PCPV)
    1. Introduction to Pharmacovigilance (PV) and Risk Management
    2. Standard Terms and Definitions
    3. Global Perspective of PV and ADR Reporting
    4. Guidelines and Standard Governing PV
    5. Global AE Reporting System and Reporting Forms
    - US FDA Form 3500 and 3500A
    - Medicines and Healthcare Products and Regulator Agency's Vigilance Reporting Form-Yellow Card
    - Medeffect Canada and Canada Vigilance Program
    - Suspected Adverse Drug Reaction Reporting (SADRR) Form
    - Universally Accepted ADR Reporting Form CIOMS I Form etc.
    6. Individual Case Safety Reports (ICSRs)
    7. Medical Dictionary for Drug Regulatory Activities (MedDRA)
    8. Periodic Safety Update Reports (PSURs)
    9. Expedited Reporting and Requirements
    10. PV Inspection and Compliance Monitoring

    READ MORE >>>

    Jobs & Opportunities after PDCR & PCPV
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    Clinical Research Associate (CRA), Clinical Research Coordinator (CRC), Clinical Data Manager (CDM ), Drug Safety Associate (DSA) etc.

    Highlights of PDCR and PCPV Programs:
    Ease of Training and Evaluation: Distance learning mode and Assignments based evaluation
    Optimal Duration: 6 months
    Course Fee: Rs. 9600 each (DD in favour of Catalyst Clinical Services Pvt. Ltd. payable at Delhi)
    Last Date of Enrolment: 10th February 2014

    Follow the links below to download the Application Form. Our placement assistance can also be viewed on the same link,

    << DOWNLOAD APPLICATION FORM FOR PDCR >>

    << DOWNLOAD APPLICATION FORM FOR PCPV >>

    Enrolment Procedure:
    In order to enrol, one simply needs to send us the duly filled Application Form (available at the links above), copy of highest qualification certificate and DD of prescribed fee to the address mentioned in the footer of the Application Form.

    Advantages of PDCR and PCPV Programs:
    - Increases the visibility of your CV
    - Equip you with the required knowledge to handle the potential interview questions
    - Wide recognition and acceptance of the program(s) throughout the industry
    - Placement assistance via regular job postings on CR Network

    Contact Details:
    Catalyst Clinical Services Pvt. Ltd.
    Corporate office:
    503, NDM-2, Netaji Subhash Place, Pitampura, Delhi – 110034, India
    M:
    +91 9818356273; Ph: +91-11-45121445, 45121435
    Email
    : info@catalystclinicalservices.com

  • Career for B.Pharm/B.Sc as Production Executive (Injactables)-Contact Manufacturing

    Leading pharma co. with huge range of products ranging from sterile preparation to oral solid dosage forms with international markets.

    Post: Production Executive (INJECTABLES)-Contact Manufacturing (1 opening, Male Candidate Only)

  • RASA LSI ,Pune inviting application for Research trainee/industrial training/Projects in Bioinformatics, Chemoinformtics, Drug Designing, Microarray data analysis,molecular modelling and dynamics || 100% job guarantee program in Software Development

    We are a leading BCIL (Biotech Consortium India Ltd) recognized and CRISIL rated organization located in Pune which deals in providing the high quality R&D services and training in the area of Life Science informatics like Bioinformatics, Cheminformatics and BIO-IT.

  • PHARMACOLOGICAL ACTIVITIES OF BENZIMIDAZOLE- A REVIEW

    About Authors:
    Narinderpal Kaur*, Annapurna Negi, Jyotsna
    Assistant Professor
    School of Pharmacy and emerging Sciences
    Baddi University of Emerging sciences and Technology
    Baddi, Himachal Pradesh
    *narinder.sonia@gmail.com

  • Admission opportunity in B.Pharm and M.Pharm at Lovely Professional University

    Pharmacy is a dynamic, growing, and increasingly diverse profession, one which creates an excitement because there are so many opportunities for service. The secret in the future will be to identify and take advantage of these opportunities.

  • Shoolini University offers admission for B.Pharmacy, M. Pharmacy (Pharmaceutics, Pharm. Chemistry, Pharmacology, Pharmacognosy, Quality assurance, Biotechnology), B. Pharm MBA (Integrated), and PhD programs

    Shoolini University is is located in a thick grove of pine trees, 14 km from Solan with cool summers and pleasant winters, and an ideal destination for academic and research romance. It has adopted research driven model and its strength emanates from Sound Governance and Cultural Heritage. Governing Body is comprised of distinguished academicians, entrepreneurs, professional executives and consultants.

  • Multiplace vacancies as MRO in SCM (3 posts) - Kazadores

    A leading Pharma major client of Kazadores,

    Post: MRO in SCM , 3 posts

  • Opportunity to get Training for Medico-Medical Writing in Tulip Medcom

    Medical writing is part and parcel of drug development process. Medicomarketing communication or healthcare communication has evolved as a profession over a decade. More and more pharmaceutical industries are outsourcing their work to medicomarketing communication or healthcare communication companies/freelance medical writers.

  • Work as DGM-US Market ( Regulatory Affairs ) in Trueosis Consultancy

    Trueosis ever since its inception in 2007 has been involved in providing high quality manpower solutions and services. We have been successful in providing consistent and reliable services to our customers who include BFSI, BPOs, ITIndustries, Pharma, Private Manufacturing Enterprises and FMCG Companies.
    The culture at Trueosis is based on strong interaction with customers in order to provide complete satisfaction in terms of desired output.

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