Clinical Trial Application (CTA) Submission in India
We at WorkSure™ support in preparation of Clinical Trial Application and related documents viz. Investigator’s Brochure, trial protocol, case report form, informed consent form, patient information sheet, EC submission document etc. WorkSure™ also provides technical expert representation to undertake discussions with regulatory authority.
Clinical Research Organization in The Field of Clinical Research
Clinical Research Organization industry is possibly the most booming area of the bio services industry. Collection and validation of clinical trials data play an essential role in pharmaceutical, biotechnology and medical device research.
WorkSure, Clinical Research Organization in India, supports clinical research and clinical data management services in all phases of trials
WorkSure, Clinical Research Organization in India, supports clinical research and clinical data management services in all phases of trials
Medico Marketing Shall Avoid Misleading Advertisements And Disease Mongering
Medico marketing involves
promotion of pharmaceutical products. It facilitates to continuously update physicians,
nurses and pharmacists regarding the safe and effective use of medicines.
Medico marketing encompasses activities by medicos or organizations to
actualize markets for pharmaceutical care.
The World Health Organization defines pharmaceutical promotion as “all information and persuasive activities executed by pharmaceutical manufacturers and distributors, attempting to affect the prescription, supply, purchase, and/or use of medical drugs”.
The World Health Organization defines pharmaceutical promotion as “all information and persuasive activities executed by pharmaceutical manufacturers and distributors, attempting to affect the prescription, supply, purchase, and/or use of medical drugs”.
What is Clinical Data Management Services ?
Clinical Data management Services is collected, integration as well as validation of clinical trial data. Clinical Data manager manages many clinical trial data including security and efficacy data of drugs/agents within the study. All data coming from CRF from sites (hospitals/clinics) and non-CRF data coming from clinical laboratories. Collect and validate the trial data, review as well as querying the investigators, and quality assurance on the trial data, etc.