Bloomsbury Clinical Research has extensive experience in preparing and submitting initial clinical trials applications to the regulatory bodies and ethics committees within and outside the UK.  Our service includes but is not limited to:

• attending independent ethic committee review meetings

• writing patient recruitment materials including informed consent forms

• preparing and submitting substantial and non-substantial amendments to the regulatory bodies and/or ethics committees

• preparing and submitting annual progress reports and end of study notifications

 

Please contact us in order to discuss your needs and we will do our best to support you.