Thao Ngo Email & Phone Number | Currently, i am at the position of RA Executive in CKD Pharm. With the experience of nearly 10 years in both main job Regulatory Affair and other tasks, I believe that i can handle multi-tasks as: - Meet with foreign partner for seeking supplier of drug substances. Check COAs/ DMF of many API manufacturer and get decision to choose which manufacturer based on quality (specification) and price. - Get plans of registered products directly from the board of Director, seek outsourcing pharmaceutical factory and research which new product can be produced at which factory. - Assign and manage the compiling product registration (new registration/ supplement registration/ variation/ extension) of many partner/ manufacturer as well as compile all type of product registration, product import quota by myself and submit to DAV all of them to keep up company’s schedule. - Follow up the period of re-registration, planning, and make the preparation of dossiers for re-registration/ extension registration of product. - Work with all department (QA, QC, RD, RA) to control process of development new product until the dossiers submitted on time and combine with them in factory to handle the production plan to keep up marketing plan. - Follow up the process of MOH' s appraisal dossier in detail and push the expert who is in charge of the dossier to push visa number out or the approval letter. - Contact with DAV, Health department, Testing Institute for BE study, testing sample, building up specification and validation, solving problems as Withdraw of drug product. - Participate in training, seminars, conferences, professional training of the company and outside activity. - Looking for the foreign partners and making contact through mail/ phone to seek the chance of cooperation with them in distribution of imported products (drug products/medical devices/cosmetic product) which are appropriate with the strategy of business development. For further information, please don’t be hesitate to contact me through my email address thaongo1311@gmail.com or my phone number 0937.242.994.

Thao Ngo

Currently, i am at the position of RA Executive in CKD Pharm. With the experience of nearly 10 years...
Vietnam

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Thao Ngo’s Email thao@ckdpharm.com

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Thao Ngo’s Location Vietnam

Thao Ngo’s Current Industry Chong Kun Dang Pharm

Thao Ngo’s Prior Industry Brv Healthcare | Medbolide Pharma | Ymed | Shinpoong Pharmaceutical

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Work Experience

Chong Kun Dang Pharm

RA Executive

2020-09-01 00:00:00 - Present

Brv Healthcare

Assistant

2020-07-01 00:00:00 - 2020-08-01 00:00:00

Medbolide Pharma

Regulatory Affairs Specialist

2018-03-01 00:00:00 - 2020-07-01 00:00:00

Ymed

Regulatory Specialist

2017-01-01 00:00:00 - 2018-02-01 00:00:00

Shinpoong Pharmaceutical

Regulatory Affairs Associate

2011-02-01 00:00:00 - 2016-12-01 00:00:00

Skills

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Languages

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FAQ About Thao Ngo

Thao Ngo is located at
Vietnam

Thao Ngo is a Currently, i am at the position of RA Executive in CKD Pharm. With the experience of nearly 10 years in both main job Regulatory Affair and other tasks, I believe that i can handle multi-tasks as: - Meet with foreign partner for seeking supplier of drug substances. Check COAs/ DMF of many API manufacturer and get decision to choose which manufacturer based on quality (specification) and price. - Get plans of registered products directly from the board of Director, seek outsourcing pharmaceutical factory and research which new product can be produced at which factory. - Assign and manage the compiling product registration (new registration/ supplement registration/ variation/ extension) of many partner/ manufacturer as well as compile all type of product registration, product import quota by myself and submit to DAV all of them to keep up company’s schedule. - Follow up the period of re-registration, planning, and make the preparation of dossiers for re-registration/ extension registration of product. - Work with all department (QA, QC, RD, RA) to control process of development new product until the dossiers submitted on time and combine with them in factory to handle the production plan to keep up marketing plan. - Follow up the process of MOH' s appraisal dossier in detail and push the expert who is in charge of the dossier to push visa number out or the approval letter. - Contact with DAV, Health department, Testing Institute for BE study, testing sample, building up specification and validation, solving problems as Withdraw of drug product. - Participate in training, seminars, conferences, professional training of the company and outside activity. - Looking for the foreign partners and making contact through mail/ phone to seek the chance of cooperation with them in distribution of imported products (drug products/medical devices/cosmetic product) which are appropriate with the strategy of business development. For further information, please don’t be hesitate to contact me through my email address thaongo1311@gmail.com or my phone number 0937.242.994.