Safety Services

Product Description

Navitas Life Sciences can help you create and implement an effective lifecycle benefit-risk strategy to ensure patient safety, as well as to keep your products on the market. Navitas Life Sciences has defined and upheld PV compliance with more than 40 life sciences companies to date. We know the future of drug safety and we believe in transforming performance and compliance by improving processes to get you there.

Navitas Life Sciences

  • DE
  • 2015
    On CPhI since

Navitas Life Sciences

  • DE
  • 2015
    On CPhI since

More Products from Navitas Life Sciences

  • Clinical Services

    Product Clinical Services

    As a proven full services provider, Navitas Life Sciences brings our rich experience from partnering with well over a 100 innovator and generic Life Sciences companies to conduct a significant number of studies, including Phases 2 – 4, NIS, Biosimilars, and BA/BE. We have been a partner of choice for bringing several life-saving drugs to market, and have worked across several therapeutic areas, with significant expertise in Oncology. Our expertise also encompasses stem cell therapies, and diagnostic imaging and contrast agents. With a global workforce of domain experts attuned to industry trends, we bring significant subject matter expertise, regulatory strategy for product development, audit ready infrastructure, a skilled and experienced delivery team, and technology platforms that ensure compliance and are genuinely architected to enhance efficiencies and reduce costs.
  • Consulting Services

    Product Consulting Services

    At Navitas Life Sciences our experienced consulting team delivers strategy and change management programs to our clients. We are a leading life sciences consultancy with global reach and some 25 years of experience. We are proud of our track record of results with clients focusing on Patient Safety, Risk Management, and Quality and Compliance.

    Our team of 50+ industry consultants cover strategy, people, process, and technology. With clients in over 50 pharmaceutical, medical device, biotechnology, and consumer health organisations we are experienced in supporting focused remediation projects and large scale transformation programs.

  • Industry Networks

    Product Industry Networks

    Our nets community is the place to discuss trends, insights, and future solutions. The philosophy behind each network is to:

  • Provide a platform for industry peers to learn and share from one another in an open environment
  • Deliver benchmark information to compare and measure operational and organisational performance
  • Discuss key issues facing organisations with ‘hot topics’ addressed by action teams
  • Regular forums to derive best practices to develop innovative future solutions to tackle shared challenges
  • Provide access to the latest industry insights through webcasts, think tanks, and community exchange
  • Offer satellite working sessions to surface industry trends and explore future strategies to boost performance and success
  • Aimed at pharmaceutical industry professionals, the networks were founded as an independent community for business leaders facing similar challenges to have a peer network to exchange insights, compare performance, and debate strategies to tackle the latest hot issues. Each network has a focused and evolving agenda to meet the latest challenges.
    Our networks span across the Clinical, Regulatory and Safety verticals, covering topics like pharmacovigilance, Regulatory Information Management, Labeling, and the role of the CMO.

  • Regulatory Services

    Product Regulatory Services

    As experts with more than 100,000 regulatory submissions under our belt, 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. We offer unit-based pricing, which is our unique outcome-based engagement structure where clients pay in line with the submission workload. Our lean, reliable, and cost-effective partnership model is designed to ensure a smooth approval process while optimizing costs, accelerating time-to-market, and reducing risk of non-compliance/de-licensing.

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