Pharma Research, provides exceedingly reliable inputs for the intend of safety management plans that are complete study specific, with the help of a highly committed and experienced group of Safety Physicians, thereby ensuring there is a regular and accurate reporting and processing of AE’s & SAEs, with compliance to the regulatory guidelines.

The safety management services of Pharma Research include:

Reproductive Endocrinology

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Neurology

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Any successful clinical trial depends highly on amethodical feasibility and site selection. At Pharma Research, the center of our proposal activity and project planning is the feasibility process. Almost every area of the medical sector has been worked on by the feasibility group at Pharma Research. We also are in direct contact with the trail sites and important investigators.

The feasibility assessment process that we follow at Pharma Research ensures, proficient identification of finest investigative sites that are worth conductingclinical trial, and thus provide highly effective results.

Our dedicated team has vast experience in coordinating phase II to IV trials on both national and international scales. We can perform all stages of clinical trials – from feasibility to final study report – to the highest quality standards.

We have wide therapeutic experience, excellent cooperation with site staff, and in-depth knowledge of local requirements. Our core expertise and focus is in the South and South East Asia, however we are able to cover the whole of Asia and many other countries through our partner CROs. Our resourcing model provides both the flexibility and local knowledge of each country that the study requires.

Monitor plays a significant role to ensure the project success.  As a company commitment to Clinical Research Excellence, we designed the role of our monitors to go beyond, than simply meeting the technical accuracy demanded by the research.

Our CRAs are trained to predict site management issues and proactively develop and implement solutions. CRAs undergo a thorough instructional regimen and are trained. This approach is employed from the earliest stages and throughout the conduct of the clinical study, to ensure the proper flow and responsiveness of the process.

All our monitors are full-time bilingual employees, equipped with laptops and are always available through mobile phones and internet when they are off site.

Whether helping your organization handle an overload of work on a single project or designing a full-service clinical program for your product, Croissance clinical trials management team has experience and knowledgeable staff members ready to assist you.

• Clinical services custom-tailored to fit your needs.
• Study document development.
• CRA management and quality control.
• Clinical monitoring and site management.
• Clinical Trial Management System.
• Investigator meeting planning.
• Third party vendor management.
• Audits and preparation for audits.
• Training.
• Patient recruitment and retention strategies.
• Feasibility studies.
• Quality training of clinical associates.