Bangalore

Job opening for M.Pharm, B.Pharm as Technical Data Associate (67 posts) at CDSCO - Government of India

CENTRAL DRUGS STANDARD CONTROL ORGANIZATION, Under the Drug and Cosmetics Act, the regulation of manufacture, sale and distribution of Drugs is primarily the concern of the State authorities while the Central Authorities are responsible for approval of New Drugs, Clinical Trials in the country, laying down the standards for Drugs, control over the quality of imported Drugs, coordination of the activities of State Drug Control Organisations and providing expert advice with a view of bring about the uniformity in the enforcement of the Drugs and Cosmetics Act.

Become a Job Ready Professional for Clinical Research Industry, Join Reva University Recognized program in Clinical Research

  • Posted on: 21 June 2019
  • By: admin

 

Rukmini Knowledge Park,
Kattigenahalli,Yelahanka, Bangalore - 560064

Admission open for "Post Graduate Diploma In Advanced Clinical Research and Management" of Pharma, Life Science and Medical Graduates

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Clinical Research Industry has grown around the world at an unparalleled rate in the past few years. It has opened up new vistas of employment for a large number of people in India as well. It is one of the most knowledge-intensive industries and complete biography of drug from its inception in the lab to its introduction to the consumer market and beyond. Clinical Research is a systematic study to evaluate the effectiveness and safety of medications or medical devices by monitoring their effects. Clinical research has become a multi-billion and multidisciplinary industry. A number of factors favor India as a clinical research hub.

 

About the University
REVA University has been established under the REVA University Act, 2012. The University is located in Bengaluru on a sprawling green campus, spread over 45 acres of land, built with state-of-the-art infrastructure creating an environment conducive to higher learning and research.

 

Program Specialty

  • Clinical Research Outsourcing
  • Implementations of electronic records in Clinical Trials
  • Enabling an integrated clinical enterprise
  • Efficient IT support
  • Course Content
  • Clinical Trial Management
  • Clinical Data Management
  • Pharmacovigilance
  • Medical Writing
     

Career Opportunities
The exposure to advancing technology and an impressive career growth progression of Clinical Research, makes considering careers in Clinical Trials and Clinical Research worth it, especially for individuals with Pharma and Life science backgrounds in:

  • Clinical Operations
  • Clinical Data Management
  • Quality Assurance
  • Pharmacovigilance
  • Business Development
  • Regulatory Affairs
  • Medical Writing

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Eligibility
- Pharma Students B.Pharm/ M.Pharm/ Pharm.D- M.Sc./ B.Sc. [Life Sciences)
- Graduate and Post Graduate in: Biological sciences [Microbiology, Biotechnology, Biochemistry, Zoology), Nursing (B.Sc. M.Sc.), Physiotherapy(BPT/ MPT)
- Engineering Graduates (B.E, B.Tech, M.Tech in Biotech)
- MBBS/ BDS/ BAMS/ BH MS etc.-Candidates with Graduate/ Post Graduate qualifications in Medical and allied Fields like Dentistry, Homeopathy, Ayurveda and Veterinary Science and Pharmacy.

 

Duration :
- 2 Semesters
- 7 Months of Classroom Training +3-4 Months of Project Work

 

Potential Employers
❖ Contract Research Organizations
❖ Pharmaceutical Companies
❖ IT Companies
❖ Premier Hospitals

Immediate Job Profiles
- Clinical Research Coordinator / Clinical Research Associate
- JRF / SRF
- Pharmacovigilance Scientist
- Drug Safety Associate
- Clinical Data Associate / Data Process Associate
- Medical Coader
- Document specialist
- Regulatory Affairs

 

Project work -
To fulfil the program requirement. PGDACR is divided into 2 Parts - Classroom + Dissertation work. Dissertation program will be For three months; will be conducted at Clini India, Bengaluru Campus. Participants will undergo an extensive program in Clinical Research & Clinical Data Management.

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Contact:
Reva University
Rukmini Knowledge Park,
Kattigenahalli,Yelahanka, Bangalore - 560064
Site: www.reva.edu.in
Ph: +91 95388 74444
admissions@reva.edu.in

CLICK HERE TO FILL ONLINE APPLICATION FORM

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Job Openings for M.Pharm, B.Pharm as Bench Chemist (197 posts) at CDSCO - Government of India

CENTRAL DRUGS STANDARD CONTROL ORGANIZATION, Under the Drug and Cosmetics Act, the regulation of manufacture, sale and distribution of Drugs is primarily the concern of the State authorities while the Central Authorities are responsible for approval of New Drugs, Clinical Trials in the country, laying down the standards for Drugs, control over the quality of imported Drugs, coordination of the activities of State Drug Control Organisations and providing expert advice with a view of bring about the uniformity in the enforcement of the Drugs and Cosmetics Act.

For engaging outsourced manpower in various categories CDSCO under the MH&FW have selected the following agencies through GeM as per procedure.

Vacancy for Territory Business Executive at Pheasantz | 04 posts

Pheasantz though is a MSES organisation yet is backed up with more than two decades of valuable industry experience, building innovative dermatology brands in collaboration with expert panel of medical and non-medical customers. Pheasantz believes in bringing together a competent team of external and internal resources from different background, to work collectively with clear intent to discover an unmet need and formulate a product which satisfies the same.

Post : Territory Business Executive  - 04 post

Walk in interview for M.Pharm, B.Pharm, M.Sc in Quality Control, Quality Assurance, IPQA, Microbiology at Stelis Biopharma

Stelis Biopharma Private Limited (Stelis) is a vertically integrated biopharmaceutical company with R&D, process scale up and end –to- end manufacturing capabilities from drug substance to finished drug products in all injectable formats. Stelis has a state of the art research facility in Bengaluru along with a soon-to-be commissioned 200,000 square feet integrated bio-manufacturing facility catering to biologic APIs and injectables conforming to international standards. The principal shareholders of Stelis are Strides Pharma, Tenshi Life Sciences Private Limited ( Integrated Life Sciences Company) and GMS Holdings ( Group of diversified business and assets with a strong biopharma franchise in the MENA region).

Admission open for B.Pharm, M.Pharm at Nirma University

Dear Student,

Institute of Pharmacy, Nirma University received All India Rank # 21 for year 2019 by the National Institutional Ranking Framework (NIRF), MHRD, Government of India.

Nirma University is one of India’s leading universities based in Ahmedabad (Gujarat). The University was established in the year 2003 and recognized by the University Grants Commission (UGC) under Section 2 (f) of the UGC Act. Nirma University is accredited with ‘A’ Grade by National Assessment and Accreditation Council (NAAC).

Institute invites applications from eligible candidates for following programs.

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Admission 2019
Institute invites applications from eligible candidates for following programs.

[1] B.Pharm. – Approved by Pharmacy Council  of India (PCI)

As per ACPC, Gujarat State Norms

  • 85 Seats - admission through ACPC, Gujarat
  • 15 Seats - admission as NRI Seats by Nirma University
  • 05 Seats ​- (Supernumerary/Additional) for Tuition Fee Waiver (TFW) Scheme to be filled by ACPC, Gujarat
  • 15 Seats - (Supernumerary) as PIO, GULF, FN, CIWGC-SEA Quota – filled by Nirma University (Refer for more details - http://www.nirmauni.ac.in/NU/gulf_pio)

​Admission to B.Pharm. Program would be as per the Norms of ACPC, Gujarat State (http://www.jacpcldce.ac.in/)​

Website : http://www.nirmauni.ac.in/IPNU/BPharm_Admissions

[2] Master of Pharmacy (M.Pharm.) – Approved by Pharmacy Council  of India (PCI)

Total 69 seats

  1. Pharmaceutics - 15 seats
  2. Pharmaceutical Chemistry - 15 seats
  3. Regulatory Affairs- 12 seats
  4. Pharmacology- 12 seats
  5. Pharmaceutical Analysis- 15 seats

Stipend would be given to All MPharm Students
GPAT Qualified Student : Rs. 12,400/- per Month
Non-GPAT Student : Rs. 5,000/- per Month

Last Date to Apply Online : 10th June, 2019

Website : http://www.nirmauni.ac.in/IPNU/MPharm_Admissions

[3] Executive Diploma Program in Pharmaceutical Management (EDP-PM)

  • Special Program for Working Professionals
  • Minimum Two years of Professional Experience in appropriate field
  • 33 Sundays, 3 Terms with 3 Courses in Each

For more details, Visit - http://www.nirmauni.ac.in/IPNU/EDP_Admissions
Email : admission.edpip@nirmauni.ac.in

 

Other information about Institute as follows...

Unique Features

  • Highly Qualified Faculty members
  • Well-Equipped Laboratories
  • More than 8 Crore Funded Research Projects
  • Publications in Reputed Journals
  • Excellent Placement Records
  • MoUs with Leading Research Organizations
  • Collaborations with International Universities

Placement Records of Previous years. - http://www.nirmauni.ac.in/ipnu/AboutPlacementCell

Details of Faculty Members  - http://www.nirmauni.ac.in/IPNU/Faculty

 

Apply Online for Our Website

Admission Coordinator,
Institute of Pharmacy, Nirma University,
Sarkhej - Gandhinagar Highway,
Ahmedabad - 382481, Gujarat - INDIA
Tel : 079-30642715
Email : admission.ip@nirmauni.ac.in
Website: www.nirmauni.ac.in/IPNU/Admissions

Find us at Facebook

Instagram : nirma_pharmacy_official
Twitter : @IPNUOficial

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Build career in Clinical Research with Clini India. Join Advanced Program in Clinical Research & Management. Admissions Open for June, July and August 2019

MODULES YOU WILL LEARN:
Clinical Trial Management
Clinical Data Management
Pharmacovigilance
Medical Writing

 

UPCOMING BATCHES

Batch Dates June 19 July 19 August 19
 
Pune 24 Jun 23 Jul 27 Aug
Mumbai No Seats 7 Jul / 30 Jul 20 Aug
Hyderabad 24 Jun 22 Jul 19 Aug
Bangalore 27 Jun 23 Jul 20 Aug
 
Online 27 Jun 26 Jul 27 Aug

 

PLACEMENTS:
In the last batch, the Institute has witnessed the participation of many Life Science students and professionals now working with Fortune 500 and global CRO, Pharma and IT Companies  more details - Click here

<<CLICK HERE, IF YOU WISH TO GET PROGRAM DETAILS>>

<<CLICK HERE TO VISIT WEBSITE>>

 

THE INDIVIDUAL EFFECT OF SURFACTANTS ON THE PENETRATION OF GLIMEPIRIDE TRANSDERMAL PATCHES USING DIBUTYLPTHALATE AS A PLASTICIZER

ABOUT AUTHORS
P.Mounika, Dr Rinku mathappan, Sukriti Vishwas
Gautham College of Pharmacy, Bangalore – 560032

ABSTRACT

Objective
Glimepiride is an anti-diabetic drug with shorter half-life of 5 hrs. Glimepiride penetration into skin is difficulty. To study effects the penetration of glimepiride using different surfactants using dibutylpthalate.

Methods
Glimepiride transdermal Patches are prepared by using solvent casting method.  Eudragit E -100, Polysorbate 80, Polysorbate 60 are used as a penetration enhancers. Dibutylpthalate acts as a plasticizer for the penetration enhancement.

Results
The present study was to formulate and evaluate transdermal drug delivery system of Glimepiride. Results were evaluated for Thickness, Tensile strength, Folding endurance, and Drug content and In vitro penetration study was performed by using Franz diffusion cell. The drug content in transdermal patch F-1 shows 98,F-2 shows 93, F-3 shows 92.the drug permeation through matrix membrane shows good release with Eudragit E-100 copolymer and surfactant SLS. In comparison with three surfactants SLS gives good release for glimepiride with Eudragit E-100 matrix membrane.

Conclusion
From the results glimepiride with SLS anionic surfactant shows good penetration. Dibutylpthalate acts a plasticizer which improves the penetration of glimepiride.

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