Sheetal Mudda

Sheetal Mudda Email and Phone Number

Global Regulatory affairs Manager at Micro labs @
Sheetal Mudda's Location
Mumbai Metropolitan Region, India
Sheetal Mudda's Contact Details

Sheetal Mudda work email

Sheetal Mudda personal email

n/a
About Sheetal Mudda

Sheetal Mudda is a Global Regulatory affairs Manager at Micro labs at Micro labs. She possess expertise in anda, pharmaceutical industry, regulatory affairs, regulatory submissions, generic programming and 26 more skills. Colleagues describe her as "Sheetal is very nice person to work. She is part of my team, is highly focused and dedicated. She attains perfection towards her work through sincere efforts I wish her very best and successful career in future"

Sheetal Mudda's Current Company Details
Micro labs

Micro Labs

Global Regulatory affairs Manager at Micro labs
Sheetal Mudda Work Experience Details
  • Micro Labs
    Global Regulatory Affairs Manager
    Micro Labs Jul 2007 - Present

Sheetal Mudda Skills

Anda Pharmaceutical Industry Regulatory Affairs Regulatory Submissions Generic Programming Gmp Pharmaceutics Ectd Cleaning Validation Formulation Regulatory Requirements Change Control Validation Glp Dissolution 21 Cfr Part 11 Capa Ctd Fda Pharmacovigilance Sop Technology Transfer Abbreviated New Drug Application Drug Delivery Gcp Gxp Hplc Ich Gcp Pharmaceutical Research Pharmacology V&v

Sheetal Mudda Education Details

Frequently Asked Questions about Sheetal Mudda

What company does Sheetal Mudda work for?

Sheetal Mudda works for Micro Labs

What is Sheetal Mudda's role at the current company?

Sheetal Mudda's current role is Global Regulatory affairs Manager at Micro labs.

What is Sheetal Mudda's email address?

Sheetal Mudda's email address is ad****@****ail.com

What schools did Sheetal Mudda attend?

Sheetal Mudda attended University Of Mumbai, Topra Spring Introductory Course, London.

What skills is Sheetal Mudda known for?

Sheetal Mudda has skills like Anda, Pharmaceutical Industry, Regulatory Affairs, Regulatory Submissions, Generic Programming, Gmp, Pharmaceutics, Ectd, Cleaning Validation, Formulation, Regulatory Requirements, Change Control.

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