Krushangi Patel Email & Phone Number
@takeda.com
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Who is Krushangi Patel? Overview
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Krushangi Patel is listed as Director, GRA CMC Submissions Management at Takeda at Takeda, based in Dracut, Massachusetts, United States. AeroLeads shows a work email signal at takeda.com and a matched LinkedIn profile for Krushangi Patel.
Krushangi Patel previously worked as Director, GRA CMC Submissions Management at Takeda and Associate Director, GRA CMC Submission Management at Takeda. Krushangi Patel holds Graduate Certificate, International Biopharmaceutical Regulatory Affairs from Northeastern University.
Email format at Takeda
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AeroLeads found 1 current-domain work email signal for Krushangi Patel. Compare company email patterns before reaching out.
About Krushangi Patel
1) Tenacious, proactive, and dedicated team player with positive attitude, and a desire to succeed 2) Exemplary interpersonal and communication skills
Listed skills include Ectd, Anda, Fda, Isi Toolbox, and 32 others.
Krushangi Patel's current company
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Krushangi Patel work experience
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Associate Director, Gra Cmc Submission Management
Senior Manager, Global Regulatory Affairs- Cmc Submission Management
Manager, Global Regulatory Affairs- Cmc Submission Management
Regulatory Affairs Associate Iii
Regulatory Associate Ii
- Collect, verify, classify and prepare records for all or parts of regulatory ANDA submissions, annual reports, materials and other regulatory agencies for various markets for Transdermal Drug Delivery products to.
- Collecting and compilation of data for submission of Deficiencies.
- Evaluation and preparation of Post-approval supplements ((PAS, CBE/CBE-30) to manage regulatory product life-cycle.
- Writing, Revision, and control of Standard Operating Procedures.
- Assist in review of change control forms.
- Assist in product launch activities.
Regulatory Affairs Associate Ii
- Compiling and reviewing ANDA’s, amendments, deficiencies, Supplements (PAS, CBE/CBE-30), annual reports for US Market.
- Involved in technical review of submissions including complex drug products.
- Evaluating changes to regulatory documents, FDA guidance’s and formulating strategies to achieve timely submissions and expedite approvals in accordance with current requirements of the agency.
Regulatory Associate
1)Worked in Post Approval Department - Mostly timely preparation and electronic submission of annual reports and Paper submission of ADE Reports.2) Reviewing supplements and change control forms.3) Maintaining company's databases4) Worked on some part of ANDA Modules5) Knowledge about Ectd and ESG Gateway systems. 6) Knowledge about ISI Writer and ISI.
Krushangi Patel education
Graduate Certificate, International Biopharmaceutical Regulatory Affairs
Ms Of Regulatory Affairs, Pharmacy Administration And Pharmacy Policy And Regulatory Affairs
Bachelor'S Of Pharmacy, Pharmacy
Frequently asked questions about Krushangi Patel
Quick answers generated from the profile data available on this page.
What company does Krushangi Patel work for?
Krushangi Patel works for Takeda.
What is Krushangi Patel's role at Takeda?
Krushangi Patel is listed as Director, GRA CMC Submissions Management at Takeda at Takeda.
What is Krushangi Patel's email address?
AeroLeads has found 1 work email signal at @takeda.com for Krushangi Patel at Takeda.
Where is Krushangi Patel based?
Krushangi Patel is based in Dracut, Massachusetts, United States while working with Takeda.
What companies has Krushangi Patel worked for?
Krushangi Patel has worked for Takeda, Amneal Pharmaceuticals, Aveva Drug Delivery Systems (An Apotex Company), and Apotex Inc..
How can I contact Krushangi Patel?
You can use AeroLeads to view verified contact signals for Krushangi Patel at Takeda, including work email, phone, and LinkedIn data when available.
What schools did Krushangi Patel attend?
Krushangi Patel holds Graduate Certificate, International Biopharmaceutical Regulatory Affairs from Northeastern University.
What skills is Krushangi Patel known for?
Krushangi Patel is listed with skills including Ectd, Anda, Fda, Isi Toolbox, Regulatory Submissions, Microsoft Office, Powerpoint, and Regulatory Affairs.
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