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Services
Pacific-Link offers a wide range of drug development and business development services to our clients. Our approach is to provide clients with a single point of contact for project management and contractual relationships to conserve our customer.s resources. Our network of affiliates has expertise in almost every area of pharmaceutical and biotechnology development. Pacific-Link Consulting Services has offices in San Diego, California and Tokyo, Japan. Though our collaborative relationships, our representatives can provide services to clients across the US, EU (London) and Japan (Tokyo).
Pacific-Link offers our clients expert service in developing Regulatory Strategies, Quality Systems, Biostatistics, Medical Writing, Clinical Trials (Phase I/II), electronic Common Technical Dossier Submissions (preparation of Regulatory materials and electronic publishing), Pharmaceutical Development and Audits (both GCP and GMP expertise). Pacific-Link also specializes in licensing and venture capital due diligence assessments of products and companies. The services listed below are representative of what Pacific-Link can offer clients seeking drug development support. Don’t see what you are looking for below? Please contact us with any special needs to see if Pacific-Link can assist or we would be happy to help find the appropriate expert to support your company’s important projects.
Regulatory Strategy Support - Pacific-Link offers senior level regulatory support to develop the right Regulatory Strategy for your development projects
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Regulatory Submission Support - Our expert Regulatory staff can prepare, review and file regulatory submissions and provide a wide range of services to facilitate registration of drug products with health authorities Worldwide
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Clinical Development - Pacific-Link can support client’s needs in clinical research though our collaborative efforts.
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