Clinical Research Center What is clinical research?
Non biologics - Development costs and timelines Opportunities and Challenges with Biologics Clinical Development of Biologics — how is it different?
New clinical trials rules and its impact Current requirements of Indian Clinical Trial Application CTA and how this will change with the new clinical trial regulation Substantial amendments and non-substantial amendments Ethical considerations for clinical trials performed in children guideline compared with adults Influencing the best strategy for the different regulations across India and globally Key development for sponsors and investigators to insure if they meet regulatory necessities when performing multi-country clinical trials Conducting direct-to-patient trials using technologies, such as apps and wearables to report data and analyse current strategies and relevant regulations Assuring the efficacy and success of clinical trials — What is a best practice for working with regulatory agencies?
Promoted as Joint Commissioner in March Expert in Detection and investigation of various cases related to spurious drugs and other violations of Drugs and Cosmetics Act. He began his career as a lecturer at J. College of Pharmacy, Ooty.
He was awarded as "Best Drugs Inspector" in the year He has made remarkable contributions in National and International seminars, workshops, which shows his urge for upgrading knowledge of the complex pharma spectrum which undergo rapid changes. Mayur Parmar is working as Deputy collector with Govt of Gujarat.
He is carrying six years of rich experience and during his tenure he has inspected various Drug manufacturing sites, drugs Distribution sites, hospitals, blood banks and blood storage centres as per Indian as well as WHO guidelines.
With six years of experience of Drug Regulation, Mayur has investigated more than NSQ drugs and launched Prosecution for spurious and misbranded drugs.
Prior to it Mayur has completed his M. Pharm with specialization in New Drug Delivery System from Maharaja Sayajirao university of Baroda, Gujarat with two gold medals for securing first rank in the university.
He has published four research papers in International and National journals. His views on Pharma regulations have been published in various magazines like eHealth and others. He is pursuing his Ph. D in New Drug Delivery System.
He has chaired two international conferences and speaked at various national and international forums. He is having industrial experience in formulation development and Intellectual property management.
A Huge believer of lifetime learning - Mayur constantly strives to improve himself, both on personal and professional front. He has managed clinical development of novel molecular entities in diverse therapeutic areas in all clinical development phases.
Dr Bhatt has worked as a consultant in pharmaceutical medicine and clinical pharmacology. Dr Bhatt is the recipient of Drug Information Association outstanding Service award for his immense contributions in his field of specialization. Dr Bhatt has more than publications in national and international journals.
In this role, he is responsible for managing scientific and medical affairs for the regions of Asia, Latin America, Africa, Middle East and Eurasia.Peter Kotanko, MD as the Research Director is responsible for the overall direction of RRI’s research whose work spans bench science to clinical research to epidemiology to mathematical modeling, protocol design, manuscript preparation and teaching.
The Clinical Trials Research Associate (CTRA) curriculum prepares individuals to assist investigators and clinical researchers in the initiation, administration, coordination, and management of clinical research studies for the development of new drugs, clinical products, and treatment regimens.
Veeda Clinical Research is an Independent CRO which offers a fully integrated package to its clients for studies ranging from PK studies in healthy volunteers to patient trials for generics, NCE and Biopharmaceutics. Grant award stimulating research at health professional academic institutions with not more than $6 million per year of NIH support in total costs in each of four or more of the last seven years.
The Epilepsy Foundation’s Clinical Trials Portal connects participants to current trials and observational studies to help accelerate development and testing of new treatments.
Clinical Research Organization Business Plan. Do you want to start a clinical research business, and need a clinical research organization business plan to help you successfully launch your operation?
It is true that writing a business plan is critical in helping you secure funding for a business and even to get it started the right way.