About CRO in Russia - Clinical Excellence Group (CEG)

Based in Russia and working with global companies we bring best practices to research that are based on ethical behavior, quality assurance and first class service.

CEG team is consisted of professionals experienced in working with international companies and educated in the reputable Russian and international universities.

We are proud that a young and ambitious company can make a change in research and positively impact patients' lives.

We ground our work by doing the right thing and assuring each step is made in the right direction.

Therefore, we created and follow our
CEG Ethical Code.

✔ We abide the local laws and global guidelines.
Our reputation is the key and each step matters. CEG high compliance standards ensure that all routine practices have a solid legal background and leadership team is involved in general guidance and detailed instructions.

✔ We strictly follow the principle: Do not harm. We carefully gather info about all side-effects and treatment outcomes.
Trials are conducted to help patients live longer and obtain better quality of life - this goal is always kept in our mind. We believe that only ethical professionals can do so. CEG was established for the long-term and such principle talks by itself. Jointly with trial sponsor we carefully analyze benefits and risks for each product. CEG professionals proactively communicate their findings.

✔ Our communication with physicians, patients and clients is open and clea.
Without honesty, courage and support the result would be unattainable. We make sure every procedure is carefully communicated and all stakeholders are on the same page. Being trained all around the world we know by experience how important is to listen to each other.

✔ We always have informed consent form for the patients and ensure private information protection.
Of course, there is legal regulation that we abide to. But not less is important is trust. Trust is fundamental when it comes to health. Our partners in medical hospitals know by experience that they can trust us and patients' materials will be kept confidential.

✔ Quality assurance is in place at all stages of research and data analysis.
To make the data reliable we naturally invest in modern technology. Additionally, we are well educated in standard operating procedures. What matters most is that we apply our brains in excellent analysis once the trial moves to the final stage.

✔ Our employees are the unique resources and great personalities. Therefore, we constantly invest in growth by conducting regular trainings.
By the end of the day, we can only sell what are good at and such is our expertise. We value each other as people and professionals. We are a good team and come to work because we want and like doing it.

We want the EAEU a part of international environment and follow the highest ethical and quality standards. We can make it real by doing our everyday work.

We are Russian professionals trained in the reputable international universities. Our successful experience with reputable multinational and local companies makes us confident we understand our clients' needs and act effectively. We carefully monitor regulatory environment and conduct internal trainings.

We are:
✔ High-performing and mobile team;
✔ With excellent communication skills;
✔ Ready to assist our clients in case of challenge;
✔ We know and enjoy what we do.

Six of our specialists have more than 7 years of work experience in pharmaceutical companies and international Contract Research Organizations, four specialists have more than 12 years of experience.

Our team includes 6 unique medical writers and biostatisticians - there are only few such professionals in Russia and bordering countries.

In 2012-2017, CEG successfully passed 5 audits by international Sponsors.

Every year our company's staff takes an assessment of knowledge of Standard Operating Procedures and the legislation of Russia and the Eurasian Economic Union.

Our work is guided by standards established on the market of healthcare products registration and biomedical studies.

This goes for development and implementation of 38 Standard Operating Procedures (SOPs) and Policies, 100+ Standard Forms, Logs and Tables that regulate organization, monitoring and audit of Clinical Trials, selection of investigation sites, logistics, drug circulation, pharmacovigilance and study participants' safety, conduct of nonclinical studies, adverse event handling and many other activities.

This is an additional guarantee of your projects' success.