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    Pharma Services Category of Prorelix Research

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    01 Clinical Development / Phase IIb-IV (1)

    02 Compliance, Regulatory & Consulting (1)

    03 Early Clinical / Phase I-IIa (1)

    04 Medical Writing & Language Translation (2)

    05 Patient / Investigator Recruitment (1)

    06 Post Marketing (1)

    07 Technology / Data / Analytics (2)

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    01 Prorelix Research (9)

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    01 India (9)

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    Prorelix Research

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      PHASE I CLINICAL RESEARCH SERVICES

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      - Service Details

      At ProRelix Research, the dedicated clinical trial project management team provides Phase I to IV clinical research services in compliance with the principles of ICH & GCP, trustworthy clinical safety services and site selection.

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      Pharma Service: Clinical Trials

      Category: Early Clinical / Phase I-IIa

      Sub Category: Phase I / IIa
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        PHASE IV CLINICAL RESEARCH SERVICES

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        ProRelix Research's dedicated clinical trial project management team provides high-principled, smooth running of clinical trial operational services from Phase I to IV in India, USA, Europe and UK.

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        Pharma Service: Clinical Trials

        Category: Clinical Development / Phase IIb-IV

        Sub Category: Phase IV
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          MEDICAL WRITING & TRANSLATION

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          ProRelix Research offers various clinical trials services such as medical writing, translation of documents, insurance identifying, selecting and recruiting investigators and contracts, regulatory submissions, etc.

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          Pharma Service: Clinical Trials

          Category: Medical Writing & Language Translation

          Sub Category: Clinical Research Translation / Validation
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            SELECTION & RECRUITMENT OF INVESTIGATORS

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            ProRelix Research provides various services such as selection and recruitment of investigators, medical writing, translation of documents, submissions to regulatory authorities, etc.

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            Pharma Service: Clinical Trials

            Category: Patient / Investigator Recruitment

            Sub Category: Overview
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              CLINICAL DATA MANAGEMENT

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              ProRelix Research offers various data management & statistics services such as CRF designing/tracking, test script, discrepancy resolution, preparation of mock CRF, preparation of data validation specifications (DVS) and study-plan specifications (SPS).

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              Pharma Service: Clinical Trials

              Category: Technology / Data / Analytics

              Sub Category: Data Management
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                DATA MANAGEMENT & STATISTICS

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                ProRelix Research performs prompt services of data management, data entry, data verification, data validation specification, statistical analysis, CRF designing & tracking, discrepancy resolution along with trial reporting services.

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                Pharma Service: Clinical Trials

                Category: Technology / Data / Analytics

                Sub Category: Clinical Biostatistics and Programming
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                  REGULATORY & PHARMACOVIGILANCE SERVICES

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                  ProRelix’s regulatory & pharmacovigilance services include clinical sections of common technical documents (CTDs) & new drug applications (NDAs), risk management plans, periodic safety update reports (PSUR) along with benefit risk evaluation reports.

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                  Pharma Service: Clinical Trials

                  Category: Compliance, Regulatory & Consulting

                  Sub Category: Regulatory Affairs
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                    MEDICAL WRITING & TRANSLATION SERVICES

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                    ProRelix Research has undertaken a wide range of medical writing assignments such as protocols, clinical study reports, literature research, technical documents, case narratives, abstracts & manuscripts, investigator’s brochures (IBs), etc.

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                    Pharma Service: Clinical Trials

                    Category: Medical Writing & Language Translation

                    Sub Category: Overview
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                      PHARMACOVIGILANCE SERVICES

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                      ProRelix Research offers end to end pharmacovigilance services such as individual case safety reports writing, narrative writing, SAE reports, triage, medical review, signal detection, risk management and report submission to the regulators.

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                      Pharma Service: Clinical Trials

                      Category: Post Marketing

                      Sub Category: Pharmacovigilance / Product Lifecycle Management
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