www.novartis.com Healthcare Pvt Ltd Hyderabad : Drug Safety & Epidemiology Pharmacovigilance

[muthukalee]

novartis.com

Pharmacovigilance Leader (Drug Safety and Epidemiology)

Job ID : 79747BR
Position Title : Pharmacovigilance Leader (Drug Safety and Epidemiology)
Division : Pharma
Business Unit Pharma - Global Development
Country : India
Work Location : Hyderabad
Company/Legal Entity : India Novartis Healthcare Private Limited
Functional Area : Development & Medical
Job Type : Full Time
Employment Type : Permanent

Job Description:
Provide support to the Brand Safety Leader/Pharmacovigilance Leader (BSL-PVL) in the monitor-ing of the safety profile of assigned products including : Periodic Safety Update Report (PSUR), Risk Management Plan (RMP) updates and associated activities, safety signal detection, coordinat-ing the management of large datasets for analysis purposes , responses to external authorities, review of clinical protocols and other regulatory activities, and responsibility for the clinical review and evaluation of cases including input for follow-up and data cleaning, within agreed timeframes and to a high standard of accuracy, in compliance with IMS business rules, standard operating procedures and global and local regulatory requirements

1. Assist the BSL-PVL in monitoring the safety profile of product
2. Provide input into responses to inquiries from regulatory authorities or health care profes-sionals on safety issues
3. Provide input to responses for CPO requests involving safety issues
4. Assist in the development and updates concerning safety input to the core data sheet and the investigator’s brochure
5. Play an active role in standing and ad hoc Safety Management Team (SMT) meetings
6. Play an active role in SIGDET and MSRB meetings including preparatory activities
7. Assist with project activities on an ad hoc basis
8. Interfaces with the clinical team for safety matters including follow-up on events of interest and input into site queries regarding adverse events, updating on PVO requirements
9. Provide clinical input to detailed review of events of interest for key data extraction for analysis purposes including the PSUR and other ad hoc analyses
10. Together with the BSL-PVL, co-author the PSUR including analytical input to PSUR for known and potential risks defined in the RMP
11. Assist in the development and maintenance of the RMP including the coordination with other line functions for associated activities such as updates, management of large datasets for analysis purposes and the ongoing tracking of commitments and effectiveness measures
12. Assist in the preparation of other safety documents, as required, including the Annual Safety Update Report (ASR) and the Investigator’s Brochure (IB)
13. Participates in review of clinical study protocols reports other regulatory documents as needed.
14. Provides support as required for licensing activities, regulatory authority inspections audits and for project product recall activities.
15. Lead the training and mentoring of internal and cross-functional team members

Minimum requirements Education (minimum desirable) : Bachelor of Science in Pharmacy Bachelor of Science in Nursing PharmD PhD in relevant field or MD

Languages : Good knowledge fluency in English. Knowledge of other languages desirable.

Experience Professional requirement :
• 4-6 years prior experience in clinical research or its equivalent with a minimum of 3 years of drug safety experience preferred. May be a first job in the pharmaceutical industry for an MD with 3 years clinical experience postdoctoral
• Experience in safety document or medical writing including experience coding with MedDRA and WHO dictionaries in preparation of these reports preferred
• Excellent understanding of clinical trial methodology, GCP and medical terminology
• Attention to detail and quality focused
• Strong organizational and project management skills
• Strong negotiation and communication skills, and the ability to operate effectively in an international environment
• Excellent understanding of physiology, pharmacology, clinical study objectives, and the drug development process
• Strong technical and problem solving skills
• Good presentation skills
• Strong computer skills including, but not limited to, creation of spreadsheets, templates, presentations and working with safety databases applications.
• Ability to work independently, under pressure, demonstrating initiative and flexibility through effective innovative leadership ability.
• Ability to mentor, and coach within IMS and cross functionally
• Ability to lead global work groups
• Ability to lead and deliver initiatives

Apply Job : https://sjobs.brassring.com/2057/asp...esume.asp?SID=

Contact us :
Novartis Healthcare Pvt. Ltd.
Building # 6
Raheja Mind Space, Hitech City
Madhapur / Hyderabad, Rangareddy 500 081
INDIA
Website : http://www.novartis.com/

[Guest]

CURRICULUM VITAE
GUNDA KISHORE E -Mail : kishorecologist AT gmail.com
OBJECTIVE : A Self learning and self motivating personality with communication skills seeking a position that will capitalize on acquired knowledge, learning and experience. Desiring a position with career growth potential, to be successful professional utilizing my knowledge & skills and improve my personal traits through a growth oriented organization.
EDUCATIONAL QUALIFICATIONS :

Degree / Study Name Of The University / School Year Of Passing Percentage Of Marks
High School
(SSC) TRINITY HIGH SCHOOL, Peddapalli,
Dist. :karimnagar March 2002 84.5%
Intermediate
(Bi.P.C) {Biology,Physics,Chemistry} SRI CHAITANYA COLLEGE,Vijayawada March 2004 87.9%
Bachelor Of Pharmacy G.PULLA REDDY COLLEGE OF PHARMACY
(Osmania University)
Mehdipatnam, Hyderabad, India. 2005-2006 to
2008-2009 66.9%
Master Of Pharmacy VEL’S INSTITUTE OF SCIENCE TECHNOLOGY AND ADVANCED STUDIES 2009 PURSUING
SOFTWARE PROFICIENCY :
- Operating Systems : MS DOS, Windows 98, 2000, XP
- Packages : MS Office
SKILLS AND ABILITIES :
- Willingness to learn new technologies and skills
- Ability to tackle people diplomatically
- Team facilitator
- Timely handling of situations
CURRICULUM PROJECT :
Project Title :
In M.Pharmacy : Protective Effect Of Aqueous Extract Of Ichnocarpus Frutescens And Cyperus Rotundus Against Cisplatin induced Invivo-Testicular Toxicity In Rats.
ACHIEVEMENTS :
- Received a certificate with 46th rank at all India level in NATIONAL LEVEL
PHARMACY TALENT SEARCH EXAMINATION 2008.
- Participated in INTER COLLEGE CRICKET COMPETITION conducted at HYDERABAD.
- Received a Certificate of Excellence with Distinction in ALL INDIA GENERAL
KNOWLEDGE EXAMINATION.
LIST OF PUBLICATIONS :
- CETP Inhibitors - Upcoming strategies to treat atherosclerosis, Journal of Advances in Drug Research,Vol 1,Issue 1, Dec 2010,35-42.
POSTER PRESENTATION
- I have presented a poster on “Protective Effect Of Ethanolic extract of Cyperus rotundus Against Cisplatin induced Testicular toxicity invivo in Rats. IPS 2010” HYDERABAD. [Main author]
- I have presented a poster on “Pharmacokinetic And Pharmacodynamic Study Of Pioglitazone And Rosuvastatin Alone And In Combination Using Rats IPS 2010” HYDERABAD. [Co author]
AREAS OF INTEREST
- Regulatory affairs
- CRO
- Pharmacovigilence

[Guest]

RESUME
Naveen Raghu.R
raghu_3234 AT yahoo.co.in
________________________________________
OBJECTIVE :
To work in a research environment where I can use my talents and interpersonal skills in the innovation of new scientific things and for equipping myself with newer technologies.
SUMMARY :
- Sound knowledge and hands-on experience in synthesizing and characterization of Gold Nanoparticles conjugated with Anticancer drug.
- Good understanding of biological and nanotechnology based applications like drug delivery, Drug discovery, Drug formulation, sensors and Tissue Engineering.
- Excellent practical skills gained through academic and project experience.
- Self-motivated, with good communication and interpersonal skills.
EDUCATION :
Course Board / university Year of passing Percentage
M.Tech- Medical Nanotechnology SASTRA University, Thanjavur. June-2011 60
B.Pharm E.G.S.Pillay college of Pharmacy, Nagappattinam. April-2008 64

Technical Skills :
- Software skill :
- MS Office
- Photoshop
- Origin
- Instruments Handled :

- Viscometer,
- Particle size analyzer,
- UV spectrophotometer,
- Goniometor.

- Instrument Known in :
- SEM
- AFM
- XRD
- FTIR
- Areas of Interest :
- Health care,
- Software,
- Health Care R&D,
- Drug Discovery,

- Sensors.
- Semiconductor.
Project :
B.Pharm :
Leaf extract of thespesia populnea (L) soland is treated with anti-inflammatory and Anti convolution effect on mice
Place where project was done : E.G.S.Pillay college of Pharmacy, Nagappattinam.
M.Tech :
To Synthesized and characterization of Gold Nanoparticles conjugated with Anti cancer drug.
The Gold Nanoparticles was synthesized by chemical reduction methods, The gold Nanoparticles are conjugated to anticancer drug, The samples are characterized by UV, FTIR, SEM, EDAX. Were conform the presence of gold conjugated the anticancer drug.
Place where project was done : CeNTAB, SASTRA University, Thanjavur.

[Guest]

Dear Sir/ Mam,
I am interested in working for the organisation in order to have an opportunity to show my attributes to the industry & to learn a lot of new things.
I am associated with Novartis from past 3 years as I am working at site for various clinical projects of which Novartis is one. I have been able to maintain good reputation both personally & professionally with the personnel. Although my resume' shows a lot of details however, it'll be great if I have an opportunity of interview with you & may be able to explain myself better.
Looking forward for a reply.
best regards
Dr. Shweta Bhatia
s.bhatia09 AT gmail.com
OBJECTIVE :
To secure a challenging position that will utilize my clinical and research experience, education and unique innovative abilities to contribute to the success of the company.
SKILLS
- Proactive and diligent work ethics.
- Dynamic and adaptable to any given work environment.
- Acquired decisive and entrepreneurial leadership skills from past work experience.
- Proven site management abilities with capacity to design, plan and implement ideas from conception through completion; able to manage multiple responsibilities without compromise to detail or quality.
- Extensive Knowledge with Windows and various applications including MS Office (Word, PowerPoint, Excel, Project, Access).
- Strong customer service and interaction skills.
- Proven to be highly efficient in both a team and independent environment.
- Disciplined efficiency, organizational, and multitasking skills.
- Problem Solving Skills.
- Highly Proficient in Computer Operations.
- Strong Negotiating Skills.
RELEVANT EXPERIENCE
Clinical Research
- Hands on Experience in Monitoring of Clinical Investigations, Study Initiation, Carry over clinical study at site, Recruitment of Study subjects, Retention of Study Subjects, Study Closeout procedures in detail with the monitors & other members from sponsors.
- In depth understanding and training in the Review of the Study Protocol at site for feasibility, Processes and Procedures to ensure that all site personnel understand what is necessary to perform the study.
- Experience in all areas of research including budgeting, GCP, IRB/IEC protocol submissions, on-going regulatory and IRB/IEC phases and safety reporting to IEC, sponsors.
- Working knowledge of ICH GCP guidelines, clinical trial coordination, investigative site coordination, knowledge and understanding of FDA and TPD regulations.
. Well versed with both FDA & EMEA/EU pharmacovigilance processes. Experience in safety documentation coding with MedDRA, reporting SAEs, AEs, and SUSARs to the regulatory authorities both locally and internationally.
- Extensive knowledge in GMP, GLP, and GCP Guidelines.
. Experience in preparation & training of site SOPs.
- Accurate filing of Study Documents in Investigator Site File.
- Assist with development of new workflows to increase efficiency at site.
- Knowledge of Pharmacology for Clinical Research.
Therapeutic Areas :
Cardiovascular
Medical/Surgical
Respiratory (COPD)
Endocrinology (diabetes)
Nephrology (CKD), (CRF).
Musculoskeletal (osteoarthritis, osteoporosis, rheumatoid arthritis)
Immunology, Nutrition
WORK EXPERIENCE
(April ’08 to June ’09) Senior Clinical Research Associate.
Dayanand Medical College & Hospital, Ludhiana.
- Responsible for the operational components of Clinical Trials, depending on the assignment of clinical trials, this included all aspects of clinical trials from consent form of the patient to study close out, and data handling.
- Handled a team of 4 people in clinical research department and assisted/analyzed their work to meet organization’s objectives and goals.
- Handled various clinical research projects successfully.
- Provided training and support to the team members.
- Responsible for recruiting patients for clinical research department.
- Responsible for analyzing all the work of team members.
- Maintained a good rapport with the team members.
- Tracking of assigned clinical research projects with a focus on timelines, milestones and changes to the assigned contracts.
- Address any issues during study conduct in a timely manner with a positive approach.
- Management of trial-specific documents.
- Training and mentoring of team members; personal continued education.
(June 2009 till date) Sub-Investigator, Site Manager
Dayanand Medical College & Hospital, Ludhiana.
Management responsibilities include facilitating meetings and supervising the clinical project team. To offer direction and make critical decisions related to assigned projects. To work with other members of the sponsoring company, reporting project progress and making recommendations to align with therapeutic and organizational strategy.
- Completing CRFs & e-CRFs.
- Reporting of SAEs, AEs, and SUSARs to regulators as per guidelines.
- Reviewing safety documents on secure document exchange.
- Handling correspondence with Ethics Committee.
- Writing source documents for the patients.
- Maintaining/reporting Regulatory Documents.
- Collecting/Processing/Handling of specimens
- Dispensing & tracking study drug.
- Administering study drug
- Educating study patients
- E Data entry : wherein I am trained for Inform (Phase Forward) e CRF online & Novartis Software.
- Required to maintain complete and accurate study records.
- Training of team members from time to time as required.
Pharmaceutical Companies I have worked with are :
Novartis Pharmaceuticals, la Hoffman Roche, Servier (France), Daiichi Pharmaceuticals, Abbott Nutrition, Pharmacosmos (Denmark), Pfizer, Phonemix & other major MNCs.
ADDITIONAL WORK HISTORY
(July2005- July 2006) Ayurvedic Medical Officer Shaheed Kartar Singh Sarabha Ayurvedic Medical College & Hospital, Ludhiana.
EDUCATION
o 2006-2008 – M.Sc. Clinical Research (Cranfield University, UK)
o 2006-2007 – Foundation Course Clinical Research & Pharmacology
(ICRI, New Delhi, India)
o 2006-2007 – Post Graduate Diploma in Pharmaceutical Management
(ICRI, New Delhi, India)
o 1999-2000 to 2005 – Bachelor of Ayurvedic Medicine & Surgery (Desh Bhagat Ayurvedic Medical College & Hospital, Mandi Gobindgarh, Punjab, India)

[Guest]

CURRICULUM VITAE
RAPELLI MAHESH
E- Mail : mahesh.pharmacy.srp AT gmail.com
Objective :
To work in an organization where I can be constantly enhanced and I can contribute to the development of the organization
PROFESSIONAL EXPERIENCE :
Currently Working for GVK BIO CLINICAL RESEARCH PVT.LTD, HYDERABAD as CRA (CLINICAL RESEARCH ASSISTANT) since Jan 2010 to Till Date.
SKILLS :
- Having domain knowledge in BA/BE studies.
- Having good knowledge in Pharmacology.
- Having exposure on Bio-Pharmaceutics & Pharmacokinetics and
Pharmaceutical Technology.
- Having good knowledge in Clinical Trials.
EDUCATIONAL QUALIFICATIONS :
Course College, Board/University Percentage Year Of Passing
Certified Advance PG Diploma in Clinical Research and Clinical Data management Biorevelationz clinical Research ,Hyderabad 85% 2009
B.Pharmacy Vaageswari College Of Pharmacy (KU), karimnagar. 77%(distinction) 2008
Intermediate Paramita Jr College, Karimnagar. 84.5% 2003
S.S.C Sri Sharada Shishu Mandir High School, Mancherial. 77% 2001
Project details :
I Have done my project on “ MONITORING THE BIOAVALABILITY/BIO EQUIVALENCE STUDIES IN CLINICAL RESEARCH ORGANIGATIONS” in G.V.K Bio clinical research organization
Software skills :
- Package : Ms-Office (Creators computer pvt.ltd certified)
- Expertise in the area of Clinical Research in development of the SOP’s, Protocols, CRF’s, study reports, and various study material related to the conduct of the bioequivalence studies. Hands on setting up of the systems for BA/BE studies. Hands on the designing, conducting and monitoring of the trials and generation of the final reports as per the regulatory requirements.
- Basic knowledge on ICH, GCP Guidelines.
Job Profile :
As CRA
- Study in charge, which includes Planning and presentation of clinical research study information, Obtaining Informed Consent, Supervision of study related activities and Clinical data review (Compliance with Protocol, GCP).
- Execute the studies as per protocol, SOPs, GCP and other regulatory requirements.
- Preparation and Review of SOP’s according to the Regulatory requirements.
- Registered the volunteers to the volunteer data bank.
- Presentation of Informed Consent form to the volunteers / study subjects.
- Verifying the documentation of the Informed Consent form for each study subject.
- Monitoring of dosing, food consumption, volunteer interaction, documentation.
- Coordinating and being responsible for the designing and preparation of Clinical Study reports, Protocols and summary reports as per regulatory requirements.
- Communication of Study Updates with Investigators, Sponsor and Project management.
- Reporting of the Adverse Events and Serious Adverse Event to the Sponsor and IEC
- Co ordination with all concerned departments for proper planning & execution of studies.
- Checking the correctness, completeness, authenticity of the CRFs; recommending the required corrective actions as and when required.
- Preparation of all pre-study, during study & post-study documents related to study execution, making them ready for monitoring & audits.
- Query resolution management of the audits related to clinical aspects and other issues in coordination with quality assurance department.
- Responsible for communication of deviations with respect to the protocol, SOP’s, GCP and the applicable regulatory requirements to the investigator for taking corrective and preventive actions.
- Training of SOP’s and other study related activities to New Joiners /Trainees.
As a Q.C Personnel
- Performing additional responsibilities assigned by unit head
- To carry out QC checks of various phases of BA/BE studies as per SOPs and Protocols and report to Unit head
- Review of ICF and Protocol before submission to IEC & review of IEC approval process
- Verification of all screening data
- Checking of study requirements before starting the study
- Checking check-in, dosing, blood sample collection and sample separation
- Verification of study file, essential documents, clinical updates, raw data and study report for data accuracy
- Checking all log books related to project for completeness and correctness of entries
- Responsible for verification of study related documents for archival
Key Achievements :
- Experience in the field of clinical research -
(It includes Pivotal /Pilot BA/BE studies, Dose Escalating studies, Food Effect Studies,
Multiple dose / Steady state studies
Urine studies, Open label and double blinded studies etc).
- Goal-directed, results-oriented, professional with a strong clinical research background and education.
- Trained on ICH – GCP
Area of intrest :
- Clinical Research and Clinical Trails
- Drug Metabolism & Pharmacokinetics
- pharmacovigilence
- Regulatory affairs
ACHIVEMENTS
- Best student award 2003 intermediate in paramita jr college.
- Out going performance award in biostatistics and computer applications
(80/80)in vaageswari college of pharmacy.
- Many awards got in college sports.
STRENGTHS :
- Good hold on communication skills, writing and word processing skills.
- Good logic and reasoning to identify the strengths and weaknesses of alternative solutions, conclusions or approaches to problems.
- Good analytical skill, aptitude for problem solving and making critical decisions.
- Working under deadlines and strongly adaptable.

[Guest]

RESUME
PL.MUTHIAH
M.Pharm (Pharmacology)
Madurai, Tamilnadu
Email Id: muthu_pharmacist AT yahoo.co.in , krplmuthu AT gmail.com

PROFESSIONAL OBJECTIVE :
To work in a creative and challenging environment where I could constantly learn and successfully deliver solutions to problems.

ACADEMIC PROFILE :
M.Pharm Sri Ramakrishna institute of paramedical sciences,Coimbatore Dr. M.G.R. University 2010
78.41
B.Pharm
Ultra College Of Pharmacy,Dr.M.G.R University 2007
Madurai.
66.56

EXPERIENCE :
Currently working in JIPMER Hospital as “Technical Associate Pharmacovigilance” from Dec 2011 to till date.

Worked as “Clinical research associate” in QUEST LIFE SCIENCES from Nov 2010 to Dec 2011.

JOB DESCRIBTION (Technical Associate Pharmacovigilance) :
Working in “Pharmacovigilance Program of India” under Indian pharmacopoeia commission, CDSCO in JIPMER.
Ward rounds to the different wards of the hospital, viewing the case sheets, identifying the Adverse Drug Reactions.
Interacting with the physicians, Nurses and patients regarding ADRs
Collection of ADR reports Follow up with the complainant to check completeness as per SOPs
Assessment of ADRs with physicians
Reporting ADRs in vigiflow (WHO database)

PROJECT :
“ IN VITRO XANTHINE OXIDASE INHIBITORY AND ANTIOXIDANT ACTIVITIES OF THE LEAVES, FRUITS AND PEEL EXTRACTS OF Citrus aurantium ,Citrus limetta and Citrus limon”. (M.Pharm)
“ NOVEL SPECTROPHOTOMETRIC METHODS FOR THE ESTIMATION OF GEMIFLOXACIN IN PHARMACEUTICAL DOSAGE FORM”. (B.Pharm)

COCURRICULAR ACTIVITIES :
Training Program :
I’ve attended inplant training in the department of Quality control and Production of drug, in the company PHARMA FABRICON, Madurai and GRAY ANAN FORMULATIONS, Chennai.

Puplished paper :
1. Muthiah PL , Umamaheswari M, Asokkumar K. IN VITRO ANTIOXIDANT ACTIVITIES OF LEAVES, FRUITS AND PEEL EXTRACTS OF CITRUS. International Journal of Phytopharmacy. Vol. 2 (1), pp.1320, JanFeb 2012.
2. Muthiah PL. IN VITRO XANTHINE OXIDASE INHIBITORY ACTIVITY OF LEAVES, FRUITS AND PEEL EXTRACTS OF CITRUS AURANTIUM, CITRUS LIMETTA AND CITRUS LIMON. International Journal of Phytopharmacy. Vol. 2 (3), pp.7780, MayJun 2012.

Presented paper :
In “Periyar Recent Innovative Scientific Meet” in Trichy.
In ”Annual conferene of SRIPS (Southern Regional Indian Pharmacological Society)” in Coimbatore.
In “Indian Pharmaceutical association” Chennai.

Attended Conferences :
“Second International Conference and IndoCanadian Satellite Symposium On Pharmaceutical Sciences, Technology, Practice and Natural Health Products ” held at JSS College of Pharmacy, Ooty.
“IPGA (Indian Pharmaceutical Graduate Association) “ conference in Chidambaram.
“National Conference on Status and Prospects of Medicinal Plant Resources and Herbal technology”, conference in Madurai, sponsored by University Grant Commission, New Delhi.
“IPASF (Indian Pharmaceutical Association – Students Forum)” Conference in Mumbai.
Participated as a resource person in “Advanced Pharmacovigilance Workshop” JIPMER, Puducherry.
“7th Asian Conference and workshop on Pharmacoepimeology”, Banglore.

PERSONAL PROFILE :
DATE OF BIRTH : 25 111985
AGE : 26
SEX : Male
RELIGION : Hindu
MOTHER TONGUE : Tamil
LANGUAGES KNOWN : English, Tamil
NATIONALITY : Indian
DECLARATION :
Muthiah.PL do here by confirm that the information given above is true to the best of my knowledge.

[Unregistered]

RESUME
Suresh Patel
M.Pharm (Pharmacology)
Email : sureshpatel1612 AT rediffmail.com

CAREER OBJECTIVE :
I am seeking a position with a pharmaceutical company that allows me to apply and enhance my skills of being a Master of pharmacy. I desire to gain quality experience that helps me to take full advantage of my degree in pharmacy. In addition, I am eager to contribute my creativity and hard work towards the success of company and to the growth of the fast developing field.

Area of Interest :
Preclinical, toxicology, bioassay

Working Experience :
June 2011- Present :
Officer at “Zydus Cadila Healthcare Ltd”, Ahmedabad.
I have FDA approval for toxicological studies.

Role, Responsibility at above Mentioned Company :
Bioassay and Abnormal Toxicity Test :
- Bioassay and abnormal toxicity test of Gonadotrophin.
- Bioassay of Other party samples of Gonadotrophin such as Hucog 5000, Gonal-F, Ovumax, Ovufol Hp 150, Ovitrop, Sitrodin-Hp, Fetrigyn5000, Ovufol.
- Potency test for Rabies vaccine (PDEV and PCECV).
- Innocuity test for Rabies vaccine (PDEV and PCECV).
- Abnormal toxicity of test for inactivated trivalent Influenza Vaccine.
- To Test Potency, specific toxicity and abnormal toxicity test for Tetanus Toxoid.
- To Test Potency and abnormal toxicity test for Hib conjugated vaccine.
- To Test Potency, specific toxicity and abnormal toxicity test for Diphtheria Toxoid.
- To test abnormal toxicity test for MMR Vaccine.

Repeated dose toxicity study :
- Repeated dose toxicity study of Measles live attenuated vaccine human I.P. in Wistar rat by S.C. Route.
- Repeated dose toxicity study of Haemophilus influenza type b and Tetanus Toxoid (Adsorbed) in Wistar rat by I.M. Route.
- Repeated dose toxicity study of Haemophilus influenza type b in Rabbits by I.M. Route.
- Repeated dose toxicity study of Measles live attenuated vaccine human I.P. in Rabbits by S.C. Route

Single dose toxicity study :
- Single dose toxicity study of Measles live attenuated vaccine human I.P. in mice by S.C. Route.
- Single dose toxicity study of Tetanus Toxoid (Adsorbed) in mice by I.M. Route.
- Single dose toxicity study of Measles live attenuated vaccine human I.P. in Wistar rat by S.C. Route.
- Single dose toxicity study of Haemophilus influenza type b in Wistar rat by I.M. Route.

Biological Reactivity test :
- Biological reactivity test for plastic containers

August 2010-June 2011 :
Lecturer at “Shree Krishna institute of Pharmacy, Shankhalpur”, Becharaji.
Role, Responsibility and Designation at above Mentioned Institute
- Appointed as Biological scientist, IAEC of Animal House at SKIP, Shankhalpur.
- To deliver Lectures on Pharmaceutics, Pharmaceutical analysis, Pharmacology, Pathophysiology and Clinical Pharmacy.
- To give Practical Training in Pharmacology, Anatomy and Physiology, Pharmaceutics.

Project Work :
- Project done on EVALUATION OF WOUND HEALING ACTIVITY OF BLUMEA HIERACIFOLIA at Rofel, Shri G.M. Bilakhia college of Pharmacy, Vapi.

Role of Participatant in above Project. :
- To Administered Drug to Rat daily for 18 days by Topical Route.
- To Measure the Wound closure area and breaking strength of skin on daily Basis.
- To Observe and Document the Wound closure area.

Skill and Technique Known about Experiments :
- Operating of U.V. Colorimeters, HPLC.
- Jugular Vein and Carotid Artery Cannulation for Measurement of B.P. in Rat.
- To Study The Effect of Drugs on Isolated Tissue Preparation.
- Handling of different Animals and Techniques for Injection of Drugs to Animals.
- Techniques for Sacrifice and making Animals Unconscious.
- Techniques of the Collection of Blood Samples and Separation of Plasma from Blood.

Professional Achievements :
- Stood 1st University Rank in M.PHARM.
- Qualified GATE-2008, with 91.86%.

Pharmacy Profile :
Master of Pharmacy :
College/ Institute :Rofel,Shri G.M. Bilakhia college of Pharmacy,Vapi.
Exam Year of passing Percentage Grade
Second Year 2009-2010 74% Distinction
First Year 2008-2009 71.5% Distinction

Bachelor of Pharmacy :
College/ Institute :Rofel,Shri G.M. Bilakhia college of Pharmacy,Vapi.
Exam Year of passing Percentage Grade :
Final Year 2007-2008 72.15% Distinction
Third Year 2006-2007 71.2% Distinction
Second Year 2005-2006 71.7% Distinction
First Year 2004-2005 65.6% First

Educational Trainings and Seminar Attended :
- Anhils Parenteral pvt Ltd, Patan, Gujarat, India.
- 26th annual conference of Indian pharmacological society, March 2008, Vapi.
- 27th annual conference of Indian pharmacological society, March 2009, Rajkot.
- National Academy of Medical Sciences (India) sponsored Symposium on “Emerging trends in clinical trials and clinical research : Role of clinician and pharmacologists”, October 2007, Ahmedabad.

Key Strengths :
- Hard Working, Peaceful and Personal Drive and Commitment to achieve results.
- Sound Technical Aptitude with an Eye for detail and Commitment to producing Quality Work.

Pre-Pharmacy Studies :
Course S.S.C. H.S.C. :
Year of passing March-2000 March-2002
Percentage 82.29% 77.55%
Grade Distinction Distinction

Personal Details :
Date of Birth : 16th December, 1986
Marital Status : Single
Language Known : English, Gujarati, Hindi
E-mail Id. : sureshpatel1612 AT rediffmail.com