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    Looking for Pharmaceutical Services offered by TFS International AB? Find Clinical Trials for Compliance, Regulatory & Consulting to address your drug delivery challenges on PharmaCompass.

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    TFS International AB

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      PRODUCT DEVELOPMENT CONSULTING

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      The TFS Global Clinical Development Team provides strategic advice on clinical development. TFS’ team of specialists in clinical development, early phase development, regulatory affairs, and medical experts in a broad range of therapeutic indications support our customers in their clinical

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      Pharma Service: Clinical Trials

      Category: Compliance, Regulatory & Consulting

      Sub Category: Consulting Services
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        PROTOCOL DESIGN

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        The TFS Global Clinical Development Team provides strategic advice on clinical development. TFS’ team of specialists in clinical development, early phase development, regulatory affairs, and medical experts in a broad range of therapeutic indications support our customers in their clinical

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        Pharma Service: Clinical Trials

        Category: Compliance, Regulatory & Consulting

        Sub Category: Clinical Trial Design
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          REGULATORY AFFAIRS STRATEGY

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          The TFS Global Clinical Development Team provides strategic advice on clinical development. TFS’ team of specialists in clinical development, early phase development, regulatory affairs, and medical experts in a broad range of therapeutic indications support our customers in their clinical

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          Pharma Service: Clinical Trials

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          Sub Category: Regulatory Affairs
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            PREPARATION & SUBMISSION OF CTA/ITA, IND, PMA / 510 (K)

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            The TFS Global Clinical Development Team provides strategic advice on clinical development. TFS’ team of specialists in clinical development, early phase development, regulatory affairs, and medical experts in a broad range of therapeutic indications support our customers in their clinical

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            Pharma Service: Clinical Trials

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            Sub Category: Quality & Compliance
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              INTERACTION WITH REGULATORY AGENCIES WORLD-WIDE

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              The TFS Global Clinical Development Team provides strategic advice on clinical development. TFS’ team of specialists in clinical development, early phase development, regulatory affairs, and medical experts in a broad range of therapeutic indications support our customers in their clinical

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              Pharma Service: Clinical Trials

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              Sub Category: Regulatory Affairs
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                ORPHAN DRUG DESIGNATIONS

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                The TFS Global Clinical Development Team provides strategic advice on clinical development. TFS’ team of specialists in clinical development, early phase development, regulatory affairs, and medical experts in a broad range of therapeutic indications support our customers in their clinical

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                Pharma Service: Clinical Trials

                Category: Compliance, Regulatory & Consulting

                Sub Category: Regulatory Affairs
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                  PEDIATRIC INVESTIGATIONAL PLANS (PIPS)

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                  The TFS Global Clinical Development Team provides strategic advice on clinical development. TFS’ team of specialists in clinical development, early phase development, regulatory affairs, and medical experts in a broad range of therapeutic indications support our customers in their clinical

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                  Pharma Service: Clinical Trials

                  Category: Compliance, Regulatory & Consulting

                  Sub Category: Consulting Services
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                    GLOBAL QA & COMPLIANCE

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                    At TFS we strive to ensure costs are kept within the budget using our in-depth knowledge of international and local regulatory requirements and our network of global investigators to ensure that the trial objectives will be met on time.

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                      QUALITY ASSURANCE

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                      TFS Quality Assurance (TFSQA), an independent group within TFS, is responsible for ensuring the quality of the work provided by TFS, and that all work is conducted in compliance with applicable GxP guidelines, relevant regulatory requirements and applicable Standard Operating Procedures (SOPs).

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