Pharmatrial is a reliable partner that could provide in-depth regulatory support saving you valuable time and money assisting you in fulfillment of the regulatory requirements. Our well established experience and expertise in regulatory affairs, for more than a decade, in a large variety of projects and vast experience in interactions with the regulatory authorities may accelerate the approval process and reduce time to market.


Audits are an essential quality tool for verifying compliance, vendor qualification, good practices (GxP) and progress of the product development plan. In addition, they are often the first step to developing an action plan in areas where "continuous improvement" or deficiencies already known to exist.

Medical Writing is an integral part of clinical research. Our Medical Writers work closely with our colleagues in the bio-statistical, pharmacovigilance, project management, and clinical data management teams to deliver accurate, timely, and cost effective documents to the highest ethical and scientific standards.


Our Clinical Research Associates (CRAs) are highly trained professionals will coordinate clinical activities and are also experienced in providing comprehensive clinical site and study monitoring services for the client's clinical research efforts as well as regulatory support and compliance services. 

Our clinical monitoring and CRA management services include:

  • Site selection and provide feasibility research report

  • Review of inclusion exclusion criteria and the proper consenting of all subjects

  • Site selection and qualification visits

  • Assist with obtaining approval from local Ethics Committees and Institutional Review Board

  • Reporting subject recruitment

  • Review of quality systems at the site and ensuring all sites are “audit ready”

  • Initiation, interim monitoring, and study closure visits

  • Essential document review, collection, and processing

  • Good Clinical Practice monitoring, including motivational and training visits

  • Source documentation review, CRF review and query resolution

  • Accountability for all study documents and materials

  • Communication with sites

  • Study specific training to site personnel

  • Review of Investigational Product accountability and storage

  • Review of safety information of all subjects

  • Logging and correcting protocol deviations

  • Monitoring study progress

  • Mass mailings and newsletters to sites

  • Database locks and study close out of sites

We are Professional Congress Organiser has an excellent knowledge of the business tourism market and its multi tasked managers. We offer several services: advice, management and co-ordination of administrative and operational aspects of the event, budgetary monitoring,  oversee full range of services.

Pharmatrial Healthcare IT Services are designed to connect productivity with care by increasing usability, enhancing performance, and optimizing a solution’s return on investment.

Main Events:

  • International Professional Training Seminar

  • Scientific Advisory Board Meeting

  • International Scientific & Acadamic Conference

  • International & Regional Investigator Meeting in Clinical Research

Service Management Include"

  • event planning & research reports for sponsors

  • communicating with a well-respected speakers and faculty management

  • marketing commercialization of the exhibition spaces,

  • the registration of congress visitors, accommodation, travel management , abstract & presentations and the development of the scientific program

  • integrating the graphic design aspects to assigned project

  • audio-visual recording / technology integrated into  "IT Technology"

  • online event management system ( e.g . Learning Management System)

  • video tutorials development / customized  development 



  • Online School Development ( Learning Management System)

  • Web Solution ( Content Management Services)

  • Audio & Video Recording,

  • Customized Course Material Development

  • Graphic Design & IT Content Design