Monday, 8 July 2024

Clinical Trial and Complete Clinical Data Management by WorkSure

 WorkSure offers Clinical trial & Complete clinical data management services with Structured and scientific approach to protocol designing, development of a data management plan, health outcome analysis, final reporting, statistical and medical writing support.


hashtagclinicaltrial hashtagclinicaldatamanagement hashtagmedicalwriting hashtagscientificwriting hashtagdatamanagement

View more at: https://youtu.be/Y5It6ld3XWM
Read More at: https://www.worksure.org/pages/clinical-trial-clinical-data-management/



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Saturday, 6 July 2024

Medical Affairs Management by WorkSure

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Tuesday, 1 February 2022

Gigantic Influences of Medical Affairs in Healthcare Industry

 Medical Affairs are departments within pharmaceutical and medical device companies responsible for communicating accurate information to healthcare providers. Medical Affairs acts as a bridge between the industry and the broader community of healthcare providers. This department is responsible for managing external relationships with major thought leaders in the scientific community across a wide range of therapeutic fields, as well as patient groups, authorities, and other stakeholders. 

Medical Affairs in Healthcare Industry

WorkSure® Medical Affair services include medico-marketing and business development, medical communication, medical education and training, clinical research and regulatory activities, as well as KOL management and interfacing responsibilities. WorkSure® Medical Affairs service provides a comprehensive solution for pharmaceutical and healthcare organizations that deal with customers, patients, regulatory authorities, and doctors. With years of experience in therapeutic-based practices, our experienced team is well suited to assist our global clients with day-to-day challenges in the pharmaceutical industry. WorkSure® strives to meet the needs of its clients and provide complete product support.

Read more at https://lnkd.in/gyM55BqA

#medicomarketing #medicalaffaris #kolmanagement #medicaleducation #medicalcommunications

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Friday, 31 December 2021

Happy New Year 2022


WorkSure wishes everyone Happy New Year 2022

#contractresearchoganization #clinicaldatamanagement

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Saturday, 14 November 2015

Pharmacoeconomics: quantify the value of pharmacotherapy through balancing costs and outcomes

Pharmacoeconomics (PE), a sub discipline of health economics, evaluates the behavior of individuals, firms, and markets relevant to the use of pharmaceutical products, services, and programs, and with the focus on the costs (inputs) and consequences (outcomes) of that use. Cost-minimization analysis, cost-effectiveness analysis, cost-utility analysis and cost-benefit analysis are the four techniques commonly used for economic evaluation, but vary in measurement of value of health benefits and outcomes. PE assessment of formulary actions has become a standardized part of many pharmacy and therapeutic committees (PTC). PE studies are also helpful in fixing the price of a new drug and re-fixing the price of an existing drug, finalizing a drug formulary, creating data for promotional materials of medicines, compliance of requirement for drug license, including a drug in the medical/insurance reimbursement schemes, introduction of new schemes and programs in hospital pharmacy, drug development and clinical trials PE has use in health policy decision making and can be applied by a number of healthcare professionals such as policy makers, primary healthcare providers, health-care administrators, and health managers.

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Monday, 5 October 2015

Excellence in regulatory documentation rendered by medical writer

Regulatory Medical writing is an activity of writing scientific documents which are pivotal for the approval of any new drug or device. A team of specialized medical writers are involved in the preparation of Investigational Medicinal Product Dossier (IMPD), Clinical Trial Application (CTA), Common Technical Document (CTD), Investigational New Drug (IND) & New Drug Application (NDA). The regulatory medical writers must have the good knowledge of new and changing global regulations and ICH guidelines to meet the requirement of sponsor. At WorkSureTM we have the capability to work for regulatory framework of various countries including USA, Canada, Europe, Japan, India etc.

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Industries are helping medical research and communication activities

Newer treatments and bettering healthcare services are increasing life expectancy with improved quality of life. Various pharmaceutical, biotech industries and medical service KPOs are stepping forward to facilitate delivery of evidence based health care to the patients. WorkSure™, a growing name in healthcare KPO, has taken FMRC (Facilitated Medical Research Communication) initiative to help bridge the gap and increase India's share in biomedical research. This unique program is specially designed for assisting the Healthcare Fraternity to promote medical research at the level of hospitals, clinics as well as individual physician. WorkSure™ also promotes public private partnership in medical research and drug development.

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