Jasbir Chohan (Director)
Jasbir Chohan is the Founder and CEO of ONIX and has over 20 years in the pharmaceutical industry. Jasbir started the company in 2010 and has established a worldwide customer base. In 2013, Jasbir was selected for the Business Management Programme Scholarship by University of College London (UCL) and Goldman Sachs for 10K Small Business.
Jasbir has a vast knowledge of eCTD Global Regulatory Operations Requirements and has worked in Industry until transitioning to Consultancy in 2007. Jasbir is regularly invited as a key speaker at educational training programmes and conferences.
Jasbir specialises in supporting companies looking to develop or transition their regulatory operations to an eCTD compliant infrastructure, alongside this she provides an oversight for PDF publishing, eCTD compilation tasks and quality assurance compliancy for electronic submission procedures and processes.
Fun fact: Jas is a Jubilee River kayaking veteran!
Navila Rehman (Senior Principal Consultant)
Navila graduated from the University of Bradford with a BSc in Pharmaceutical Management, solidifying her place within the pharmaceutical industry for the last 20 years. With a strong background in Quality Management, Navila is the analytical problem solver of the team and has used this skill to benefit both pharmaceutical companies and CROs.
Navila joined ONIX in 2013 and has since successfully provided clients with varied submission consultancy advice and project management on global eCTD regulatory operations.
Navila is experienced in all aspects of e-submission publishing and over the years has overseen the submission and life-cycle management of countless eCTD submissions to health authorities around the world.
Fun fact: Navila can deadlift 100kg!
Emma Knight (Publisher)
Responsible for the co-ordination, preparation and publishing of electronic (eCTD) regulatory submissions for global application types. Emma has around 6 years experience working in PDF publishing and eCTD submission management, and 20 years experience working in the Pharmaceutical industry overall. With a pharmaceutical administrative background, Emma has a keen eye for detail and is overly proficient in the area of document formatting and process documentation. Emma has been a very dependable team player at Onix since 2014, being involved with a large number of different submission types on a regular basis, Emma has a clean and proven track record.
Fun fact: Emma is UK weekend-getaway expert!
Vindhya Nalagatla (Publisher)
Responsible for the co-ordination, preparation and publishing of electronic (eCTD) regulatory submissions for global application types. Vindhya has around 10 years experience working within the pharmaceutical industry, joining the Onix team in 2015. After 5 years being on the team, it is evident Vindhya brings a speed and turn around time that is second to none, expertly efficient at all stages of the submission process from compilation to submission. Vindhya has experience with many different submission types and hence a very supportive subject matter expert, ensuring clean validations and always meeting deadlines on time, every time.
Fun fact: Vindhya travels in search of new recipes to add to her healthy life style recipe list!
ONIX has an in-house team of regulatory operations experts who are highly experienced and well trained in global electronic regulatory requirements and publishing.
ONIX has an established network of CROs and Independant Consultants across Regulatory, Clinical and Quality who we work very closely with to support client’s needs. Please contact us for further information.