Instructor: Dr. Tejaswini
Validity Period: Lifetime
Are you the one who is still unaware about most demaned professional skill in Pharma industry then surely you should attend this workshop where you will get to know complete industry reqirement of:
Day1- Clinical research
The field of Clinical research offers lucrative job opportunities now and in the foreseeable future. It is one of the booming industries where recent graduates and experienced candidates can find rewarding careers.
Excellent communication skills, attention to detail and data analysis, Organizational and time management skills, and the ability to think on one’s feet are few of the skills one needs to be successful in this field.
If you possess these skills and want to make a difference in the field of healthcare then a career in Clinical research is apt for you.
The scope of pharmacovigilance grows as the array of Medicinal products expands. The rate at which new drugs are introduced and the need to continuously monitor the existing drugs has created a need for highly skilled pharmacovigilance and drug safety professionals. The pharmaceutical companies, IT industry, CRO, etc are continuously on a hunt for talented and skilled professionals in Pharmacovigilance.
Day3- Drug regulatory affair
Regulatory Affairs is a comparatively young, multidimensional and growing profession in the Pharmaceutical field with a desire to protect public health. DRA assures safety and efficacy of pharmaceuticals products, veterinary medicines, medical devices, pesticides, agrochemicals, orphan drugs, cosmetics and complementary medicines.
As outsourcing of jobs to India is high, the regulatory affairs industry in India is poised for rapid growth which is associated with flamboyant salaries. There are 120+ pharma companies having structured regulatory affairs department in India. Due to the entry of MNCs in India, it is expected a requirement of 30,000 competent and trained workforce in next 5 years.
Duration: 6 hours (2 Hours per class)
All participants will get DBT recognized & NSDC approved Learntoupgrade certificate.
How to purchase the course:
Add to cart
All classes will be live interacted with the industry experienced trainer.
Industry meet curriculam only
World wide recognised certification
Missed any Class? get the recording access for the lifetime
Many publication samples will be shared
A quality industry certificate
Contact: In case any query get in touch with us on whatsapp: +91 7290079907
|Day1 : Clinical research|
|Overview of Clinical research|
|Classification of Drugs|
|Clinical trial protocol and protocol amendment|
|Clinical Trial Protocol, Audit, Monitoring and Essential Docs|
|Clinical Data Management|
|Career in Clinical research|
|Pharma industry program: Class1: CR|
|Introduction and revision of the basic concepts|
|Pharmacovigilance Reporting Database, Signal Detection,Managements and Risk Assessments & Evaluation (I) -Quality System In PV, Expedited Reporting Criteria|
|Pharmacovigilance for healthcare practitioners|
|Pharmacovigilance for regulators and the pharmaceutical industry|
|Class 2: Pharma: 17th October|
|Day3: Drug regulatory affair|
|Introduction to Drug regulatory affairs|
|Regulatory Requirements in Pharmaceutical|
|Medical Device Regulation|
|Class 3: Pharma: 18th Oct|
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