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The role of a clinical research organization is to design, implement, and monitor clinical research, collect data, analyze results and prepare reports. Pharmaceutical companies often contract CROs to help develop new products. They manage all aspects of the trial process from beginning to end, so their work is confidential and not directly used for marketing purposes for bioanalytical lab services. 

Do You Need Different Levels of CRO For Expertise? 

Some companies require more than just essential services at the low-end that include overall management, clinical trial recruitment/administration, and project management. At the high-end, they contain general management and site selection, clinical trial recruitment and administration, data management and analysis, and preparation of reports and presentations. This is especially important if there has been a prior relationship with the CRO.

The role of a CRO is to support the sponsor throughout the process from initiation to completion. This way, everyone involved (sponsors and CROs) can get what they want from each other and complete clinical research faster and more efficiently for bioanalytical laboratory services.

What Is The Role of CRO For the Pharmaceutical Industry?

The pharmaceutical company should know what they want from the CRO and  make sure that they can trust their CRO. Both parties must understand what they expect from each other  and what works best together. 

A CRO will play a vital role in the success of the pharmaceutical industry. 

Developing a new drug is a long process that can take up to 15 years or longer. In the initial stages, the pharmacological company needs to establish safety and efficacy. Next, they have to test their product on healthy volunteers and then try it on patients with specific diseases or conditions. They then need to do clinical trials that can be broken into phases where they test safety. They work toward finding a dosage, and they finish by studying the side effects and benefits of their drug in large-scale studies called Phase III studies. Only once this has been accomplished do they approach regulatory authorities for approval on the drug development process.

Is the Process of Hiring CRO Expensive?

The process is costly. At the beginning of Phase I studies, it’s estimated that it costs between $15-50 million to develop a new drug. Then depending on how far they go, they can spend $200 million on clinical trials for each planned drug. Large pharmaceutical companies find the development of new medicines financially risky, so they outsource this job to CROs that focus on clinical trials. A CRO can handle all aspects of the practice, including running the study, recruiting participants, and managing the site selection for clinical research sites.

What are the Advantages of Using CROs for Clinical Trials? 

Using CROs is similar to using contractors instead of having all employees in-house. With most CROs, any lab can be outsourced to a contract research organization (CRO). They will not be involved in the research and testing phase of clinical trials but will provide support during the initial step.


Using CROs makes the process more efficient and save time and money for both parties. Clinical trials can take months and years to complete,but CROs make it easier by  maintaining consistency throughout all phases of clinical trials. Through close collaboration with CROs, pharmaceutical companies can minimize less evident risks. In the long run, apharmaceutical company will be more successful in its drug development if its CRO works closely with them.

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