Skip to main content

Regulatory affairs

 

Clinical courses

 

Clinical research courses

  • Novo Nordisk looking for Junior Professional in Regulatory Affairs

    Novo Nordisk is a global healthcare company with 89 years of innovation and leadership in diabetes care. The company also has leading positions within Haemophilia care, growth hormone therapy and hormone replacement therapy. Headquartered in Denmark, Novo Nordisk employs approximately 33,300 employees in 75 countries, and markets its products in more than 190 countries Novo Nordisk’s B shares are listed on NASDAQ OMX Copenhagen (Novo-B).

    Post : Jr Professional

  • Walk in interview for M.Pharm, B.Pharm, M.Sc in Regulatory Affairs at Apotex

    Apotex Research Pvt. Ltd. is a wholly owned subsidiary of Apotex Inc. Canada which is a number one generic pharma co. in Canada. The position is for Bangalore location which has an R&D Centre, Manufacturing and a Bioequivalence Centre.

  • National Conference & Workshop on Optimization and Screening of Variables by DoE at SUMANDEEP VIDYAPEETH

    ABOUT SUMANDEEP VIDYAPEETH:
    SumandeepVidyapeeth was established on 17th January 2007 and is declared as Deemed to be university u/s 3 of UGC Act, 1956. The University is accredited by National Assessment & Accreditation Council (NAAC) with a CGPA of 3.53 on a four point scale at ‘A’ Grade, in the year 2015. It is a renowned Healthcare University in state of Gujarat that indoctrinates Health-care Education and Training of high merits. SumandeepVidyapeeth incorporates globally benchmarked ‘Evidence Based Education System’ in all its academic programs. With strong research culture, excellent student-centric academic ambience, well equipped Tertiary care super-specialty Hospitals and exquisitely efficient academicians & researchers, the university is constantly marching towards the summit of excellence.

  • Clinical Trial Supply Europe 2017

    Each year, over 10,000 business executives from Fortune 1000 companies attend over 80 Arena International events worldwide, addressed by over 1,700 industry leaders delivering leading edge content and discussion. We identify the pioneering case studies, innovative solutions and up-to-the-minute discussion topics that comprise programmes of wholly unbiased integrity.

    The much anticipated Clinical Trial Supply Europe conference is back! The 17th annual edition will be held once again in Barcelona on 15th-16th of March

  • Job for Regulatory Specialist at Cerner

    Cerner is the leading U.S. supplier of healthcare information technology solutions that optimize clinical and financial outcomes. With thousands of healthcare clients worldwide, Cerner Corporation (NASDAQ:  CERN), creates healthcare information technology solutions and services that connect physician offices, hospitals, clinics, laboratories, pharmacies and consumers’ homes to timely, relevant healthcare innovation.   CernerWorks’ is an ISO 9001:2000 certified organization and is one of the fast growing segments of Cerner’s business.  CernerWorks primary function is to host, manage and monitor client systems.  Additionally, CernerWorks provides disaster recovery and temp hosting services for Cerner clients.  CernerWorks' remote hosting option (RHO) provides superior performance, security, reliability, and scalability with a lower up-front financial commitment from the client by combining hardware, networking technologies, and technical expertise.  It allows healthcare organizations to leverage the most sophisticated and powerful IT solutions available today from our state-of-the-art data centers.    In support of business operations, the CernerWorks Service Improvement team provides process architecture, associate development, regulatory oversight and auditing, and metrics and reporting functions.

    Post : Regulatory Specialist

  • Working Opportunity for Drug Safety Medical Advisor at Grünenthal

    The Grünenthal Group is an independent, family-owned, international research-based pharmaceutical company headquartered in Aachen, Germany. We are an entrepreneurial specialist delivering true benefits to patients. By sustainably investing in research and development above the industrial average, we are committing to innovation in order to treat unmet medical needs and bring value-adding products to markets. Grünenthal is a fully integrated research & development company with a long track record of bringing innovative pain treatments and state-of-the-art technologies to patients.

    Post : Drug Safety Medical Advisor

  • Career in Regulatory Affairs as Senior Excutive at BioMerieux

    A world leader in the field of diagnostics for 50 years, bioMérieux is present in more than 150 countries through 42 subsidiaries and a large network of distributors. In 2014, revenues reached €1,698 million with 88% of sales outside of France.in vitro We look above all for people willing to make a commitment with us in an entrepreneurial project supported by a strong corporate culture.

  • Job for M.Pharm, B.Pharm, M.Sc in QA, QC, Regulatory Affairs at NAARI

    NAARI aspires to be a world leader in the area of female healthcare, providing medical solutions from puberty to menopause. Our aim is to be the world’s first 100% integrated generic female health pharmaceutical company. This implies complete involvement in every step of production, going from plant extract to final dosage forms. By giving our stake holders cutting edge expertise, we set the standard for female health products, globally.

  • Working opportunity for M.Pharm, M.Sc as Regulatory Affairs Analyst in Novo Nordisk

    Novo Nordisk is a global healthcare company with 89 years of innovation and leadership in diabetes care. The company also has leading positions within Haemophilia care, growth hormone therapy and hormone replacement therapy. Headquartered in Denmark, Novo Nordisk employs approximately 33,300 employees in 75 countries, and markets its products in more than 190 countries Novo Nordisk’s B shares are listed on NASDAQ OMX Copenhagen (Novo-B).

    Post: Regulatory Affairs Analyst

  • Working Opportunity for Drug Safety Specialist at Grünenthal

    The Grünenthal Group is an independent, family-owned, international research-based pharmaceutical company headquartered in Aachen, Germany. We are an entrepreneurial specialist delivering true benefits to patients. By sustainably investing in research and development above the industrial average, we are committing to innovation in order to treat unmet medical needs and bring value-adding products to markets. Grünenthal is a fully integrated research & development company with a long track record of bringing innovative pain treatments and state-of-the-art technologies to patients.

    Post : Drug Safety Specialist

Subscribe to Regulatory affairs