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    Pharma Services Category of Navitas Inc

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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 Clinical Development / Phase IIb-IV (2)

    02 Clinical Services (1)

    03 Compliance, Regulatory & Consulting (4)

    04 Core / Central Lab (1)

    05 Medical Devices (1)

    06 Regulatory Affairs / Pharmacovigilance (11)

    07 Technology / Data / Analytics (2)

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    01 Navitas Inc (22)

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    Navitas Inc

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      STRATEGIC CLINICAL CONSULTING

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      At Navitas we take a personalized approach to each client situation to ensure results are grounded in industry best-practices, but tailored to specific needs, fit-for-purpose, cost-effective, scalable, and compliant.

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      Pharma Service: Clinical Trials

      Category: Compliance, Regulatory & Consulting

      Sub Category: Consulting Services
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        MEDICAL IMAGING SERVICES

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        Navitas provides sponsors the benefit of superior image and data quality, a high degree of flexibility and customization, and validated and audited systems and technology.

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        Pharma Service: Clinical Trials

        Category: Core / Central Lab

        Sub Category: Clinical & Medical Imaging
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          BIOAVAILABILITY & BIOEQUIVALENCE STUDIES

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          With a highly qualified and experienced team in place, Navitas can deliver even complicated studies with high quality outputs.

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          Pharma Service: Clinical Trials

          Category: Clinical Development / Phase IIb-IV

          Sub Category: Bioavailability / Bioequivalence
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            BIOLOGICS & BIOSIMILARS STUDIES

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            Navitas' experience across innovator pharma and biologic Phase III studies, and pharmacokinetic studies enables us to partner with you to meet accelerated submission timelines while optimizing trial costs and regulatory risk of non-compliance.

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            Pharma Service: Clinical Trials

            Category: Clinical Development / Phase IIb-IV

            Sub Category: Bioavailability / Bioequivalence
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              CLINICAL DATA SERVICES

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              Navitas partners with you to deliver full clinical data services across Clinical Data Management, Biostatistics & Statistical programming, Clinical Data Standardization, and Medical Writing.

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              Pharma Service: Clinical Trials

              Category: Technology / Data / Analytics

              Sub Category: Data Management
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                ONECLINICAL

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                Navitas Life Sciences’ Optimized eClinical and Analytics Platform Offering Comprehensive Trial Oversight and Enabling Faster Decisions.

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                Pharma Service: Clinical Trials

                Category: Technology / Data / Analytics

                Sub Category: Clinical Biostatistics and Programming
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                  REGULATORY CONSULTING

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                  Navitas Life Sciences has the capabilities to support the regulatory end-to-end lifecycle management across the entire value chain of drug and device regulatory environment.

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                  Pharma Service: Clinical Trials

                  Category: Compliance, Regulatory & Consulting

                  Sub Category: Consulting Services
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                    GLOBAL SUBMISSION MANAGEMENT & REPORT PUBLISHING

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                    Navitas Life Sciences has the capabilities to support the regulatory end-to-end lifecycle management across the entire value chain of drug and device regulatory environment.

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                    Pharma Service: Sales, Marketing, Registration

                    Category: Regulatory Affairs / Pharmacovigilance

                    Sub Category: India
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                      CCDS, LABELING, & ARTWORK

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                      Navitas Life Sciences has the capabilities to support the regulatory end-to-end lifecycle management across the entire value chain of drug and device regulatory environment.

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                      Pharma Service: Packaging

                      Category: Clinical Services

                      Sub Category: Label
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                        LICENSE MAINTENANCE FOR MARKETED PRODUCTS

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                        Navitas Life Sciences has the capabilities to support the regulatory end-to-end lifecycle management across the entire value chain of drug and device regulatory environment.

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                        Pharma Service: Sales, Marketing, Registration

                        Category: Regulatory Affairs / Pharmacovigilance

                        Sub Category: India
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                          APPLICATION MANAGEMENT SERVICES

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                          Navitas Life Sciences has the capabilities to support the regulatory end-to-end lifecycle management across the entire value chain of drug and device regulatory environment.

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                          Category: Regulatory Affairs / Pharmacovigilance

                          Sub Category: India
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                            TECHNOLOGY

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                            Navitas Life Sciences has the capabilities to support the regulatory end-to-end lifecycle management across the entire value chain of drug and device regulatory environment.

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                            Category: Regulatory Affairs / Pharmacovigilance

                            Sub Category: India
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                              TECHNOLOGY ASSESSMENT

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                              Navitas Life Sciences has the capabilities to support the regulatory end-to-end lifecycle management across the entire value chain of drug and device regulatory environment.

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                                TECHNOLOGY SOURCING, IMPLEMENTATION, & HOSTING

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                                Navitas Life Sciences has the capabilities to support the regulatory end-to-end lifecycle management across the entire value chain of drug and device regulatory environment.

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                                  RA SYSTEM IMPLEMENTATION

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                                  Navitas Life Sciences has the capabilities to support the regulatory end-to-end lifecycle management across the entire value chain of drug and device regulatory environment.

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                                  Category: Regulatory Affairs / Pharmacovigilance

                                  Sub Category: India
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                                    IDMP READY®

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                                    Navitas Life Sciences has the capabilities to support the regulatory end-to-end lifecycle management across the entire value chain of drug and device regulatory environment.

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                                    Category: Regulatory Affairs / Pharmacovigilance

                                    Sub Category: India
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                                      RIM SOLUTIONS

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                                      Navitas Life Sciences has the capabilities to support the regulatory end-to-end lifecycle management across the entire value chain of drug and device regulatory environment.

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                                      Sub Category: India
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                                        END-TO-END PHARMACOVIGILANCE SERVICES

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                                        Navitas Life Sciences is a full-service Pharmacovigilance provider, offering Services along the PV Value chain right from Case Intake to Safety Risk Management.

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                                        Category: Regulatory Affairs / Pharmacovigilance

                                        Sub Category: India
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                                          PHARMACOVIGILANCE TECHNOLOGY

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                                          As a leading PV consulting organization, Navitas Life Sciences benefits from latest insights in the PV technology space derived from benchmarks and discussions at our industry network pvtech®, comprising of over 25 large and mid-size Life Sciences organizations.

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                                            MEDICAL DEVICES CONSULTING

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                                            At Navitas, we have a track record of successful medical device project delivery across many areas, including regulatory affairs, quality management, risk management, device vigilance and track & trace technologies.

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                                            Category: Medical Devices

                                            Sub Category: India
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                                              STRATEGIC REGULATORY CONSULTING

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                                              Navitas Life Sciences consultants which bring over 100 years of combined experience, serve as trusted advisors, providing strategic counsel backed by years of experience, industry benchmarks and insights.

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                                              Pharma Service: Clinical Trials

                                              Category: Compliance, Regulatory & Consulting

                                              Sub Category: Consulting Services
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                                                MEDICAL GOVERNANCE

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                                                At Navitas, we have worked with companies to ensure medical decisions are consistent throughout the business enabling them to approach external stakeholders with a single voice.

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                                                Category: Compliance, Regulatory & Consulting

                                                Sub Category: Consulting Services
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