Innovation for Better Tomorrow
Innovation for Better Tomorrow
About Us
Every day brings new challenges
Mediclin Clinical Research is a leading Global Contract Research Organization (CRO) based in Mumbai. We are end to end clinical trials service provider supporting comprehensive drug development and product lifecycle management. Our clients and partners include pharmaceutical, biotechnology, medical device, and government organizations.
Services
- Clinical Research Operations
- Drug Regulatory Affairs
- Pharmacovigilance
- Medical & Scientific Writing
- Clinical Data Management
- Clinical Site Management
- Data Analysis (SAS)
- Biostatistics
- Medico Marketing
Clinical Research Operations
Performance of a practical work or of something involving the practical application of principles or processes Practice until you can go through the whole operation without hesitation or thinking. An exertion of power or influence the operation of a drug.
Drug Regulatory Affairs
Drug Regulatory Affairs refers to all aspects within the pharmaceutical development process and how they are subject to various degrees of regulation. The drug regulatory affairs (RA) department of a pharmaceutical company is responsible for obtaining approval for new pharmaceutical products and ensuring that approval is maintained for as long as the company wants to keep the product on the market.
Pharmacovigilance
Pharmacovigilance drug safety is the pharmacological science relating to the collection, detection, assessment, monitoring, and prevention of adverse effects with pharmaceutical products. The etymological roots for the word “pharmacovigilance” are: pharmakon (Greek for drug) and vigilar (Latin for to keep watch).
Medical & Scientific Writing
People should know there is significant difference between Medical and Scientific writing.
Medical writing is about developing clinical and scientific documentation in a standard, comprehensive, reliable, skilled and convincing manner. Whereas scientific writing means writing about basic sciences, drugs and technological innovation for common readers.
Clinical Data Management
Clinical data management (CDM) is the process of collecting and managing research data in accordance with regulatory standards to obtain quality information that is complete and error-free. The goal is to gather as much of such data for analysis as possible that adheres to federal, state, and local regulations.
Clinical Site Management
The post involves operational management of all site issues as well as facilitating patient flow throughout the clinical areas. The post will also act as a support for both the Hospital at Night team and ward staff out of hours, to ensure the safe and effective use of resources to provide quality patient care.
Biostatistics and data analysis (SAS)
Biostatistics is a program that focuses on the application of descriptive and inferential statistics to biomedical research and clinical, public health, and industrial issues related to human populations
Biostatistics (also known as biometry) are the development and application of statistical methods to a wide range of topics in biology. It encompasses the design of biological experiments, the collection and analysis of data from those experiments and the interpretation of the results.
Biostatistics
Biostatistics mainly consists of various steps like generation of hypothesis, collection of data, and application of statistical analysis. To begin with, readers should know about the data obtained during the experiment, its distribution, and its analysis to draw a valid conclusion from the experiment.
Medico Marketing
Medico Marketing is a process of information exchange that happens between a drug manufacturer and the consulting doctor, nurse, pharmacist or with the patients. The objective of this exchange is to explain the company’s products and how it will assist the consumers in prognosis or treatment of the health related problem.
Therapeutic Expertise
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