Jasbir Chohan

WORK HISTORY

SKILLS

ABOUT JASBIR CHOHAN

Specialising in Regulatory Operations eCTD submission services. Canopy has grown a worldwide customer base of over 100 clients, delivering regulatory submissions per year to FDA, EMA, MHRA, SwissMedic, TGA, GCC & Health Canada (amongst others) with a 100% eCTD technical approval rate for electronic submissions. Alongside eCTD publishing expertise, we offer regulatory strategy consulting, submission authoring & EU Clinical Trial Regulation support including redaction services & use of CTIS. I have worked in the pharmaceutical industry for over 20 years and transitioned into consultancy in 2007 before founding ONIX in 2010. In 2013, I was delighted to be selected for the Business Management Programme Scholarship by University of College London (UCL) and Goldman Sachs for 10K Small Business. My passion, through growing ONIX Life Sciences, is to help companies simplify complex regulatory operations and speed up their drug approval process by leveraging our regulatory expertise. Small business growth | leading high performing teams | company management | regulatory affairs business development | eCTD Regulatory Operations | eCTD Lifecycle Management | e-submission consulting | Regulatory Affairs | Regulatory Operations | eCTD Publisher | eCTD compilation | eCTD Validation | eCTD Training | eCTD Strategy | eCTD working practices | MRP | DCP | CP | National | FDA | EMA | Health Canada | Swissmedic | TGA | GCC | ROW Market | ASEAN CTD | IMPD | CTA | MAA | IND | NDA | aNDA | BLA | Orphan Drug | CTD word Templates | Submission ready files | Nees/Paper to eCTD conversion | EU Clinical Trial Regulation | CTIS | Redaction