Partnering Solutions
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GMO Solutions
6/27/2023
Novotech initiated the first national, privately owned, commercial Institutional Biosafety Committee (IBC) in Australia, successfully accredited by the Australian Office of the Gene Technology Regulator (OGTR).
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Contract Dry Blending Services – API's, Excipients, Nutraceuticals
6/5/2019
The blending of APIs and excipients to create a homogenous blend is a crucial component in the solid dose and powder dose pharmaceutical manufacturing process. Because blender speed and time are key factors in achieving a uniform mixture, Ropack utilizes gold-standard technology.
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Medical Writing For Clinical Trials
1/25/2024
For successful regulatory outcomes, we provide quality medical writing services for clinical trial documents, safety updates, and marketing applications.
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Quotient Sciences Core Services
3/17/2025
Uncover how we're able to bring integrated services and trusted scientific insight to every molecule and program.
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Dual Sourcing: Mitigating Risk In Your Supply Chain
8/22/2022
Dual sourcing should be implemented to reduce risk and ensure an uninterrupted supply of critical, life-saving therapies. Recent FDA draft guidelines recommend risk management plans to prevent drug product shortages.
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How To Achieve Timely Migration Of Your TMF
9/18/2023
This precise, proven methodology delivers a high-quality migration of your Trial Master File to the destination system, typically just 4-6 weeks after receiving all documents from the source system.
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Early Phase Trials In Australia
9/6/2024
Australia is a preferred destination for early phase trials because of simple and fast regulatory stream and lucrative R&D cash refund scheme.
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Site Payments: A Better Way To Pay Global Sites
1/16/2025
This site payments solution simplifies the traditionally manual process of paying global research sites by offering a streamlined, scalable, and compliant platform.
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Clinical Trial Material Distribution Services
6/5/2019
As your clinical material partner, we simplify – and accelerate – your clinical trials. From assistance with time-consuming international documentation through destruction following all regulatory protocols, RPS is your trusted clinical trial partner.
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Expert Travel Solution For Clinical Trial Participants
7/15/2019
Getting participants to and from a research site can be burdensome for the site staff, study coordinators, participants, and their families and/or caregivers. Greenphire has designed the most comprehensive travel solution built to meet the retention goals of global clinical research.