VAIBHAV S. DALAVI vdspharma@rediffmail.

com

VAIBHAV S. DALAVI

PERSONAL PROFILE

MAILING ADDRESS: DATE OF BIRTH : 25 AUG 1984

TH

11C/ 72, MMRDA COMPLEX , CITIZENSHIP : INDIAN

DURGA NAGAR, LINK RD, GENDER : MALE
JOGESHWARI (E), MARITAL STATUS : SINGLE
MUMBAI-93 LANGUAGES KNOWN : ENGLISH,HINDI,MARATHI.
Mob-09322152070
e-mail-vdspharma@rediffmail.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. Pharma From Annamalai University, Dept of Pharmacy, Tamilnadu

B. Pharma 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 &

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@rediffmail.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. Balwant Salunke,

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

2. Mr. Amit Nakhe,

Senior CRA,
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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