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Due Diligence Services
8 services found
by:Intrinsik Inc. based inMississauga, ONTARIO (CANADA)
Product development and registration strategies; Scientific writing by qualified experts; Document authoring from source data; CTD summaries; Medical ; Nonclinical; Chemistry and Manufacturing; and, Investigator's Brochures. Data reviews and gap analyses; and,Investment due diligence (In-licensing, scientific and regulatory due ...
by:SciShield Inc. based inLebanon, NEW HAMPSHIRE (USA)
The ability to effectively put in place new operational plans for research continuity during the pandemic and to show proper due diligence in protecting your researchers is critical to your ability to keep research operations active. However, these new operational plans are plagued with implementation issues, many of which are due to the lack of ...
by:Grant Thornton Corporación S.L.P. based in50008, SPAIN
Dynamic organisations need to focus on their business' tax affairs to gain trust and stay ahead of their ...
Manufactured by:Shiphrah Biomedical Inc. based inToronto, ONTARIO (CANADA)
Research is a massive undertaking that many companies are unwilling to engage in for a variety of factors. This is especially true when it comes to women’s health research, and within women’s health, there is a long history of excluding pregnant women from clinical ...
by:BiotechExec based inAtlanta, GEORGIA (US) (USA)
Benefit from the unparalleled diversity of our Senior Executive Advisory Team (The ?SEAT’), a collective of biotech, pharma, medical device, diagnostics, and digital health specialists, who utilise their wide range of skills within the field and their shared commitment to the development of the life sciences sector, to directly benefit your ...
by:Celegence LLC based inDowners Grove, ILLINOIS (USA)
Supporting client requirements from creation to maintenance of global and local drug product labeling. Regulatory Labeling regulations are essential for ensuring compliance of drug products to be used safely and with efficacy by patients. However, regulatory labeling compliance requirements can differ across regions and new regulations are routinely being introduced to update labeling ...
by:Emergo by UL based inAustin, TEXAS (USA)
It is easy to make mistakes in the regulatory process that can delay market entry or incur unnecessary costs. With help from Emergo’s medical device RA/QA consultants, you can pursue the most efficient regulatory route to approval and registration for your device, and maintain compliance with post-market requirements ...
by:HingeClinica based inPrinceton, NEW JERSEY (USA)
HingeClinica is a world class partner for Medical Device services. We render End to End Medical device MDR compliance and Regulatory services, Clinical trial, Pharmacovigilance services to Medical Devices industry. Our Medical Device team has extensive experience in working with US FDA, EMA, PDMA, SFDA, Health Canada, DCGI and ROW, regulatory Submissions and ...