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    Pharma Services Category of TransPerfect

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    HTL Biotechnology is the world leader in the responsible development and production of pharmaceutical-grade biopolymers.
    Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
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    01 Compliance, Regulatory & Consulting (4)

    02 Medical Writing & Language Translation (3)

    03 Post Marketing (1)

    04 Technology / Data / Analytics (7)

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    01 TransPerfect (15)

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    01 U.S.A (15)

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    TransPerfect

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      PHARMACOVIGILANCE & SAFETY REPORTING

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      We enable global clinical development teams to rapidly translate and share pharmacovigilance information, such as SUSARs (suspected unexpected serious adverse reactions), SAEs (serious adverse events), hospitalization reports, and discharge summaries, within a centralized collaborative workspace.

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      Pharma Service: Clinical Trials

      Category: Post Marketing

      Sub Category: Pharmacovigilance / Product Lifecycle Management
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        CERTIFIED TRANSLATION & LANGUAGE SERVICES

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        With more than 300 drug products and vaccines currently in clinical trials, TransPerfect's expertise in medical and life science translation and language services provides the quality, efficiency, and reliability necessary to compete in this fast-paced industry.

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        Pharma Service: Clinical Trials

        Category: Medical Writing & Language Translation

        Sub Category: Clinical Research Translation / Validation
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          INTERPRETER SERVICES

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          Consecutive & escort interpretation, simultaneous/conference interpretation, remote/over-the-phone interpretation

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          Pharma Service: Clinical Trials

          Category: Medical Writing & Language Translation

          Sub Category: Clinical Research Translation / Validation
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            E-CLINICAL TECHNOLOGY SOLUTIONS

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            TransPerfect is proud to offer Trial Interactive, our 21 CFR Part 11 compliant, web-based e-clinical solution

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            Pharma Service: Clinical Trials

            Category: Technology / Data / Analytics

            Sub Category: Data Management
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              CLINICAL DEVELOPMENT DOCUMENT MANAGEMENT

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              Trial Interactive is the all-inclusive source for all of your clinical data management needs. In addition to hosting clinical trial solutions and electronic case site solutions, we also provide a full array of scanning and clinical document management services.

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              Pharma Service: Clinical Trials

              Category: Technology / Data / Analytics

              Sub Category: Data Management
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                CLINICAL OUTCOME ASSESSMENT (COA) MANAGEMENT

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                TransPerfect's multilingual e-clinical solution creates a scalable solution to securely manage Clinical Outcome Assessments and all related documentation, significantly increasing efficiencies in the clinical development and trial processes while giving secure visibility to all internal and

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                Pharma Service: Clinical Trials

                Category: Technology / Data / Analytics

                Sub Category: Clinical Trial Monitoring
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                  DUE DILIGENCE

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                  TransPerfect has developed Trial Interactive–the world's only clinical trial solution specifically designed to meet the needs of life sciences. Now, companies that are participating in licensing activities can securely share confidential product development information through an easy-to-use,

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                  Pharma Service: Clinical Trials

                  Category: Compliance, Regulatory & Consulting

                  Sub Category: Consulting Services
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                    EFEASIBILITY

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                    TransPerfect’s eFeasibility solution allows investigators to populate information into a web survey, then relaying the information to the investigators. These surveys can be done completely online or they can be printed out and done in hard copy, and uploaded via email or fax upon preference.

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                    Pharma Service: Clinical Trials

                    Category: Compliance, Regulatory & Consulting

                    Sub Category: Consulting Services
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                      ELECTRONIC INVESTIGATIVE SITE FILES (EISF)

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                      The Trial Interactive eISF offers a complete solution for electronic distribution, collection and management of essential investigator site files.

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                      Pharma Service: Clinical Trials

                      Category: Technology / Data / Analytics

                      Sub Category: Data Management
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                        ELECTRONIC REGULATORY & STUDY BINDERS

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                        Trial Interactive includes workflow to promptly facilitate the review and approval by the trial sponsor and then provides an organized, searchable electronic Regulatory Binder as well as Study Binders if required by the sponsor or institution.

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                        Pharma Service: Clinical Trials

                        Category: Technology / Data / Analytics

                        Sub Category: Data Management
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                          ELECTRONIC TRIAL MASTER FILES (ETMF)

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                          Trial Interactive provides companies with the ability to set up eTMFs in a matter of hours and can even be organized based on the file structure which is currently in place, allowing access to internal users as well as any partners with high level security access.

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                          Pharma Service: Clinical Trials

                          Category: Technology / Data / Analytics

                          Sub Category: Data Management
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                            ENDPOINT ADJUDICATION

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                            Trial Interactive provides a collaborative work space for all relevant stakeholders – including investigative site personnel, core labs, and study teams – where these cases can be collected and delivered to adjudicators.

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                            Pharma Service: Clinical Trials

                            Category: Technology / Data / Analytics

                            Sub Category: Data Management
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                              GLOBAL MULTILINGUAL CALL CENTER

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                              TransPerfect's device-independent call center solutions allow you to easily and affordably route calls to our global call centers where we intake and process cases, either as part of a clinical trial or in supporting post-marketing pharmacovigilance efforts

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                              Pharma Service: Clinical Trials

                              Category: Medical Writing & Language Translation

                              Sub Category: Clinical Research Translation / Validation
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                                LEARNING MANAGEMENT SYSTEMS (LMS)

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                                TransPerfect LMS can help you assist with meeting your global regulatory training requirements.

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                                Pharma Service: Clinical Trials

                                Category: Compliance, Regulatory & Consulting

                                Sub Category: Training
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                                  REGULATORY CONSULTING SERVICES

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                                  eCTD preparation and review, global CTA submissions, Packaging and labeling translation

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                                  Pharma Service: Clinical Trials

                                  Category: Compliance, Regulatory & Consulting

                                  Sub Category: Regulatory Affairs
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