Disha Chouhan
Name: Mrs. Disha Chouhan
Qualification: M.Pharm.
Designation : Assistant Professor
Department: Pharmacy
Institute name : School Of Pharmaceutical Science and Research, Sardar Patel University, Balaghat
College address : Balaghat
Award for : Young Achiever Award
Publication title: Conference
Paper title : Pharmaceutical Quality Assurance
Conference Name : Book publication
publication name: LAP Academic Publisher, Germany
Organizer : LAP Academic Publisher, Germany
Year : 2019
Page no. : 250
ISBN / ISSN NO.: 978-620-0-28657-4
About Disha Chouhan
Disha Patle Chouhan Assistant Professor M.Pharma(Pharmaceutical Chemistry) School of Pharmaceutical Science and Research Sardar Patel University Balaghat (M.P.) INDUSTRIAL TRAINING: One month Industrial Training at “Lupin Ltd”. (Bhopal) M.P. PROFESSIONAL EXPERIENCE: 1. ORGANIZATION: School of Pharmaceutical Science and Research (From Dec – 2015 to Till Date) DESIGNATION:- Assistant Professor 2. ORGANIZATION: ZYG Pharma PVT. LTD. Pigdamber Indore (From March – 2009 to 2013) DESIGNATION:- QA Executive JOB RESPONSIBILITIES:- 1. Product Validation 2. Qualification of Equipments 3. Stability Studies. 4. Handling Of Market Complaint 3. ORGANIZATION: ALPA Laboratories Limited Pigdamber Indore (From March – 2009 to Till Date) DESIGNATION: DRA Executive JOB RESPONSIBILITIES: 1. Preparation & Submit the Dossier as per importation & exportation requests. 2. Setting timelines for license variation and renewals. 3. Preparing and co-ordinate for various regulatory bodies for documents and keeping up to Date Company’s product range. 4. Responsible for issue of BE NOC, BA NOC, clinical trial certificate Mfg License. 5. Preparation of STP & specification 6. Preparation & Review of BMR& BPR. 7. Preparation of Process validation protocol & reports. 8. Preparation of Stability schedule, calendar, Protocols, Reports & monitoring the same & maintains record w.r.t. all activities. 4. ORGANIZATION: Acme Formulation Pvt. Ltd. Baddi (H.P.) (From Oct – 2007 to Feb 2009) DESIGNATION: QA officer JOB RESPONSIBILITIES: 1. Monitoring of in process activity. 2. Preparation of STP & specification. 3. Monitoring the issuance and retrieval of the BMR/BPR. 4. Monitoring the control sample as performing the physical tests. 5. Preparation & Review of MFR/BMR/ BPR. 6. Handling of deviation, Change control. 7. Preparation of QAR/BRR & Monthly reports. 8. Preparation of APQR. 9. Preparation of Process validation protocol & reports. 10. Preparation of Stability schedule, calendar, Protocols, Reports & monitoring the same & maintains record w.r.t. all activities. 11. SOP preparation.
Technical Skills:
1 Instrumentation : ✔ FTIR ✔ UV-Vis. Spectrophotometer ✔ HPLC ✔ Karl Fischer Titrator ✔ Bulk Density apparatus ✔ Electronic Balance ✔ pH meter ✔ Melting point apparatus ✔ Disintegration apparatus ✔ Dissolution apparatus ✔ Friability apparatus ✔ Polari meter ✔ Viscosity apparatus ✔ AUDIT& INSPECTION FACED: USFDA, TGA, MHRA, ISO, WHO, PCI, AICTE. ACHIVEMENT:- Book:- ⮚ Pharmaceutical Quality Assurance ( Lambert Publication ) Publication :- ⮚ Stability Studies in Combine dosage of Etoricoxibe & Thiocholchicoside using RP-HPLC, (IJRSB), Vol.3 Issue 9, Sep .2015. ⮚ Screening of Promising lead molecules against Two Drug targets in Ebola Virus: An Effort to Eradicate Ebola infection, IOSR Journal of pharmacy & Biological Science, Vol.10 Issue 1, Feb.2015 ⮚ Interaction of oxidative stress Responsive Gene in Cancer, Diabetes, Heart Stroke and Brain Stroke: A study to find Therapeutic Drug Target.(IJRSB) , Vol.3,Issue 8, Aug.2015. National Conference:- ⮚ “Recent Development on Pharmaceutical Formulation.” ⮚ “Emerging Changes in Phrama Industries.” ⮚ “Recent Trends and Advancement in alternative to Animal Experiments.”