SERVICES Regulatory Submissions to Competent Authority and Ethical Committees
Clinical Consulting Regulatory Affairs team
- has dedicated resources which enable us to provide regulatory solutions to suport with a wide range of regulatory affairs encountered in preparation and throughout the conduct of each clinical trial.
Clinical Consulting EU regulatory experts
- provide intelligence and strategic insight to optimize your product’s success.
Our experience includesbut is not limited to:
COUNTRY SELECTION
and local regulatory consultancy and timeline guidance
LIAISON
with local regulatory authorities, EMA agency, Institutional Review Boards, and Ethics Committees in EU countries
PREPARATION
of clinical trial authorization applications
CREATION
preparation, execution and maintenance of regulatory documents for submission to industry sponsors, ethics committees, and regulatory authorities
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If you have any concerns, we hope you’ll get in touch. We’re Here 24/7
43-100 Tychy, Poland
ul. Dzwonkowa 104
• Phone: +48 32 227 20 05
• Fax: +48 32 720 20 73
• Mail: office@clinicalconsulting.pl
• Fax: +48 32 720 20 73
• Mail: office@clinicalconsulting.pl
00-867 Warszawa, Poland
Al. Jana Pawla II 27
• Phone: +48 32 227 20 05
• Fax: +48 32 720 20 73
• Mail: rental@clinicalconsulting.pl
• Fax: +48 32 720 20 73
• Mail: rental@clinicalconsulting.pl
Subscribe To Our Newsletter
Leverage agile frameworks to provide a robust strategy