The document evaluates technology transfer approaches for solid dosage forms from R&D to manufacturing, outlining steps for effective transfer, the importance of knowledge sharing, and the impact on production quality. It highlights the aim to enhance manufacturing capacity and identifies potential gaps in knowledge required for successful implementation. The expected outcomes include adherence to WHO guidelines and various references discussing technology transfer in the pharmaceutical industry.

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Evaluation of Technology Transfer Approaches of Solid Dosage
Form, From R & D to Manufacturing Site.
Name of Student
Mr. Rakesh M. Wani
(M.Pharm IV sem)
(Department of Quality
Assurance technique)
Name of Guide
Mr. Arun M. Kashid
(M. Pharm)
(Department of Pharmaceutical
Chemistry)
STES’s,
Sinhgad Institute of Pharmacy,
Narhe, Pune - 411041

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1. Introduction
2. Literature survey
3. Aim and Objective
4. Plan of work
5. Material and Method
6. Evaluation parameter
7. Source of data
8. Outcome
9. References
CONTENT

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“The transfer of the manufacturing process for a new pharmaceutical Drug
Substance (DS) and Drug Product (DP), respectively, from the transferring site
(in this case R&D) to the receiving site or designated commercial manufacturing
site.” This includes all the associated knowledge, information and skills to be
able to manufacturing the DS and DP at the receiving site.
Introduction
Definition

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Development
of technology
by R&D
Technology
transfer
from R&D
to
production
Optimization
and
Production
Technology
transfer
documentation
Exhibit
Steps in technology transfer

6. Development of technology by R&D
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Design of procedure and
selective of excipients by
R&D
Identification of
specification and
quality by R&D
1. Step

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Technology
transfer from
R&D to
production
Master
formula
card
Master
packaging
card
Master
formula
Specifications
and standard
test procedure
2. Step

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Optimization
&
Production
Validation
studies
Scale up for
production
3. Step

9. Development
report
Technology transfer plan
Packaging development Report
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4. Steps in technology transfer4. Step

10.  Lack of manufacturing capacity
 Lack of resources to launch product
commercially
 Lack of marketing and distribution capability
 No commercial capability
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Reasons for technology transfer

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The more effectively knowledge is shared within an organization.
Innovative R&D.
Drug Approvals.
Effective commercialization.
Ensure safe, pure and effective drug product.
Cost effective production and distribution.
Advantages

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Literature Review

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LITERATURE REVIEW

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LITERATURE REVIEW

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LITERATURE REVIEW

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LITERATURE REVIEW

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LITERATURE REVIEW

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LITERATURE REVIEW

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AIM:
Evaluation of technology transfer approaches of solid dosage form, from R & D
to manufacturing site.
OBJECTIVES:
 To enhance manufacturing capacity.
 For good business and manufacturing practices.
 To transfer the knowledge throughout the organization.
 To identify the knowledge gaps that need to fill up.
AIM AND OBJECTIVE

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Plan of Work
Literature Survey
Drug excipient profile
A) Scale up batch
Experimental work
B) Exhibit batch
C) Evaluation Parameters
Data Compilation
Result and discussion
2 Month
1 Month
2 Month
1 Month
1 Month

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Drug Substance (API) and other excipients with their
manufacturer.
Material
Material and Method
Method
API and other excipients for various operation like,
Dispensing, Sifting, Mixing, Granulation, Drying, Blending,
Compression, Coating, etc.

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EVALUATION PARAMETERS

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Particle size and size
distribution
Infrared spectroscopy
X-ray powder diffraction
studies
Physiochemical study
DSC
Thin layer chromatography
Characterization of Drug sample
Organoleptic
Evaluation

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Tapped density
Carr's index
Hausner ratio
Bulk density
Loss on drying
Sieve analysis
Characterization of Powder blend

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Thickness
Hardness
Friability
Dissolution study
Disintegration study
Assay
Characterization of Finished product
Average weight

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SOURCES OF DATA
R & D documents or Transferring site documents.
Lab Note Book ( LNB)
Trade Journal
Internet Sourcing
Sources of data

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Technology transfer is important to upgrade the quality of design to be the
quality of product, and ensure stable and high quality of product.
The ultimate goal is to effectively transfer product and specification,
manufacturing and control operations.
EXPECTED OUTCOME

28. 1. WHO guideline on transfer of technology in pharmaceutical
manufacturing.
2. Gupta P, Agrawal A, Sara U, (2013),Technology transfer in Pharmaceutical
Industry, International journal of universal pharmacy and bio sciences.
2(2)93-101.
3. Gupta S, Saini S, Rana A.C., Chugh Isha, (2012), Technology transfer in
Pharmaceutical Industry, International Pharmaceutical Sciencia. 2(3)1-6.
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References

29. Kyrikos Drivas, Claire Economidou, Dimitris Karamanis, Arleen Zank,(2016),
Academic patents and technology transfer, Journal of engineering and
technology management.1-19.
Kaur A, Sharma o, (2013), Technology Transfer in Pharmaceutical Industry.
International Journal of Current Pharmaceutical Research. 5(12)1-5.
Manral M.S, Prashar B, Sheikh Y, (2012), Technology transfer in pharmaceutical
industry; Facts and steps involved. American journal of pharmaceutical research.
2(4)73-83.
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4.
5.
6.

30. Manu C, N Vishal Gupta(2016), Review on technology transfer in
pharmaceutical industry, International journal of pharmaceutical quality
assurance. 7(1)7-14
Ali s, Pandit v, Shekhar c, (2012), Technology transfer in
Pharmaceutics. International Research Journal of pharmacy. 3(6)43-48.
Chanad Sharma, (2016), R&D Technology transfer & Productivity in
the Indian pharmaceutical industry, International Journal Of Innovation
Management. 20(5)1-24.
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7.
8.
9.

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