Vaibhav S. Dalavi vdspharma@gmail.

com

VAIBHAV S. DALAVI
PERSONAL PROFILE

MAILING ADDRESS:
11C/ 72, MMRDA COMPLEX , DATE OF BIRTH : 25 AUG 1984
TH

DURGA NAGAR, LINK RD, CITIZENSHIP : INDIAN

JOGESHWARI (E), GENDER : MALE
MUMBAI-93 MARITAL STATUS : SINGLE
Mob-09322152070 LANGUAGES KNOWN : ENGLISH,HINDI,MARATHI
E-mail-vdspharma@rediffmail.com
vdspharma@gmail.com

OBJECTIVE

To become a member of the team of experts of the reputed organization. This will
provide me an opportunity to develop my skills, education for continued self growth
and enhancement of the organization in turn the nation.

ACADEMIC PROFILE

M. Pharmacy from Annamalai University, Dept of Pharmacy, Tamilnadu

B. Pharmacy from R.C.Patel College of Pharmacy, Shirpur, Dhule, Maharashtra
H. S. C. from Residential junior College, Ahmednagar, Maharashtra.
S. S. C. from B. F. High School, Ahmednagar, Maharashtra
.
INDUSTRIAL WORK EXPERIENCE

• Currently working as a CRA at USFDA approved Macleods Pharmaceuticals R n

D, Mumbai since Sept 2007.
• Industrial Plant Training: Pioneer Pharmaceuticals, Ahmednagar (1 Month).

ACHIEVEMENTS

• Faced successfully USFDA audit at Macleods R & D, Andheri.

• Faced successfully ANVISA audit at Macleods R & D, Andheri.
• Faced successfully WHO audit twice at Macleods R & D, Andheri.
• Faced successfully ISO audit twice at Macleods R & D, Andheri.
• Organized Programmes on AKASHWANI (AIR) INDIA.
• University Topper at M. Pharmacy level.

THESIS AND PROJECT UNDERTAKEN

• Completed Thesis with USFDA Approved Macleods Clinical Research, Andheri.

Topic- BABE Study of Anti-Retroviral drug
• Completed Project with Pioneer Pharmaceuticals at UG Level, Ahmednagar
• Completed Project Revised Schedule M at UG Level, R.C.P.C.O.P., Shirpur

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Vaibhav S. Dalavi vdspharma@gmail.com

JOB RESPONSIBILITIES
• Receiving Drug and Clinical trial supplies from the Sponsors and arrange for
their proper and timely distribution to the sites
• Maintaining calibration records as per GCP
• Preparing Unit Dosage forms, dispensing, archiving and retrieval of drug
products
• Maintaining the Pharmacy
• Administering drug products to subjects during clinical trials
• Verifying and Checking all Raw data before Internal QA Audit
• Sample Separation and segregation
• Writing and Revising SOPs as per need and maintain awareness of all
current SOPs
• Monitor Bioequivalence studies as per GCP and GLP
• Ensure smooth progress of the Clinical Study
• Archiving of Documents
• Assisting the Clinical Pharmacologist in SAE

REFERENCES

1. Mr. Amit Nakhe,

Senior CRA,
Macleods Pharmaceuticals R & D.,
Andheri, Mumbai.

2. Mr. Balwant Salunke,

Executive,
Macleods Pharmaceuticals R & D.,
Andheri, Mumbai.

DECLARATION

The Information furnished above is true to the best of my knowledge and I will take the
complete responsibility in case of any circumstances.

Date:
Place: Mumbai. Vaibhav S. Dalavi

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