Abhishek Ghara completed an industrial training at Gluconate Health Limited, a pharmaceutical manufacturing company in West Bengal.
[1] The company was formed through the merger of two companies in 1990 and is wholly owned by the government of West Bengal.
[2] Ghara thanks the managers and staff at the company for their cooperation and guidance during his training.
[3] He provides details of the company's production, quality control, packaging, and other departments as well as the instruments used and manufacturing processes for tablets, capsules, and liquids.
The Asian and Pacific Centre for Transfer of Technology (APCTT) is a regional institution of the United Nations Economic and Social Commission for Asia and the Pacific (ESCAP) servicing the Asia-Pacific region.
The National Research Development Corporation (NRDC) was a non departmental government body established by the British Government to transfer technology from the public sector to the private sector.
TIFAC is an autonomous organization set up in 1988 under the Department of Science & Technology to look ahead in technology domain, assess the technology trajectories, and support innovation by networked actions in select areas of national importance.
Biotech Consortium India Limited (BCIL) is a public limited company, promoted by the Department of Biotechnology (DBT), Ministry of Science and Technology, Government of India and set up by All India Financial Institutions including IDBI, ICICI, IFCI, UTI and IFCI Venture Capital Funds Limited.
Objectives, scope, Organization and structure of retail and wholesale drug store, type and design, dispensing of proprietary products, legal requirements
Pilot plant Techniques and Product consideration for liquid dosage forms.D.R. Chandravanshi
CONTENTS:-
DEFINITION
INTRODUCTION
OBJECTIVES
LIQUID DOSAGE FORM
STEPS INVOLVED IN PILOT PLANT FOR ORAL LIQUID
GENERAL CONSIDERATION
Reporting responsibility
Personal requirements
Space requirements
Review of formula
Raw materials
Relevant processing equipments
Process evaluation
GMP consideration
Assurance
PILOT PLANT SCALE UP FOR SUSPENSION
PILOT PLANT SCALE UP FOR EMULSION
REFERENCES
A platform is a group of technologies that are used as a base
or infrastructure upon which other applications, technologies
or processes are developed for the end-user.
“a common or standard method, equipment, procedure or work practice that may be applied to the research, development or manufacturing of different products ” An array of multi-disciplinary technologies covering major aspects of the drug discovery and development processes have been established in Institute of Biotechnology and Pharmaceutical Research (IBPR)
Technology Transfer Related Documents.pptxAfroj Shaikh
SlideShare Description: Technology Transfer Related Documents
Welcome to SlideShare's collection of technology transfer related documents in the field of pharmacy. This presentation focuses on the essential documentation needed for successful technology transfer in pharmaceutical manufacturing, emphasizing its role in ensuring quality, safety, and regulatory compliance.
Technology transfer plays a crucial role in the dynamic and ever-evolving field of pharmacy. It facilitates the smooth transfer of knowledge, processes, and technologies from research and development to commercial production. To ensure a seamless transition, a well-defined set of documents is required to capture critical information, procedures, and controls.
This SlideShare presentation explores the key documents involved in technology transfer within the pharmaceutical industry. The technology transfer protocol is discussed first, highlighting its purpose, contents, and significance. Acting as a roadmap, this protocol outlines the transfer scope, stakeholder responsibilities, timelines, and acceptance criteria, promoting effective communication and collaboration between the sending and receiving units.
The importance of comprehensive process descriptions is also emphasized. These documents detail the manufacturing process, equipment specifications, critical parameters, and in-process controls. They serve as a guide for the receiving unit to replicate the process accurately, ensuring consistent product quality and performance.
Validation and qualification protocols are addressed as well, highlighting their role in verifying that equipment, processes, and systems are suitable for their intended use. These protocols are crucial for meeting regulatory requirements and mitigating risks associated with the transfer.
Analytical method transfer documents are discussed next, encompassing the procedures for transferring and validating analytical methods used to assess the quality attributes of pharmaceutical products. Robust analytical methods are essential to ensure accurate and reliable test results throughout the product lifecycle.
The presentation also covers documentation related to training, risk assessments, change control, and deviation management. These documents help establish a robust quality management system, ensuring adherence to regulatory standards and facilitating continuous improvement.
Whether you're involved in technology transfer, quality assurance, or regulatory affairs, this SlideShare is a valuable resource for understanding the essential documents involved in successful technology transfer within the pharmaceutical industry. By leveraging these documents effectively, you can ensure a seamless transfer process, maintain product quality, and uphold patient safety.
Explore our SlideShare and gain the knowledge necessary to navigate the intricacies of technology transfer in pharmacy. Stay updated with the latest best practices and regulatory guidelines.
A pharmacist is the person of drugs or the expert on drugs. He is the only expert on drugs, for expertise regarding drugs requires knowledge in depth in all the facts of pharmacy. It is her professional responsibility to know all about the drugs. No educational program other than that in pharmacy provides the background to understand completely all about drugs.
Among the professions of pharmacists like community pharmacy, institutional pharmacy, whole sale pharmacy, industrial pharmacy, government service, pharmaceutical education, organizational management, in my country industrial pharmacy offers great opportunity to the pharmacists.
Industrial pharmacy is a profession of unique hybrid of business and profession.
So an industrial pharmacist should have proper knowledge about drugs and also about medical progress, commence marketing and technology. To be a self-sufficient pharmacist beside academic knowledge, practical knowledge is essential.
This is why after appearing the Bachelor of Pharmacy examination in-plant training was arranged by the department in renowned pharmaceuticals industries. This training has sharpened my academic knowledge what I learnt in the last four years .I have completed my training in Popular Pharmaceuticals Limited a fast growing pharmaceutical company in Bangladesh.
COPP/CPP it certification of pharmaceutical product for reviewing QSE i.e. Quality, Sefty,Efficacy of product. it important certification for exporting it may required by importing country.
O presente documento, GUIA REGULATORIO, visa mostrar o caminho regulatório – 2016, necessário a ser cumprido por entidades para exportação de produtos Farmacêuticos – Medicamentos, ao Peru.
Em cada slide encontram-se as informações para cada instancia no cumprimento de normativas peruanas, com links internos (hiperlinks) para abrir os documentos originais. Não todo está traduzido ao português, mas a intenção é justamente poder ter ao alcance de um simples click ou leitura compreensiva, e em forma organizada o estritamente necessário em termos legais para compor o dossiê do produto.
Arquivos contidos no paquete:
Documento principal em Power Point;
Normativas inerentes ao processo;
Documentos complementares;
Esta mesma modalidade de apresentação dinâmica pode ser extensivo para outros produtos (Biológicos, Homeopáticos, Fitoterápicos, Cosméticos, Alimentos, etc.).
Acompanha treinamento presencial ou virtual para um entendimento aprofundado de como empregar o mesmo, caso assim seja solicitado.
Este trabalho pode estar disponível, além do idioma Português, nos idiomas de Espanhol e Inglês.
Na mesma modalidade de apresentação estão disposto outros países como Argentina, Colômbia e Chile.
Para os demais países da América Latina, este trabalho se faz sobre encomenda.
Por solicitação, pode ser realizado comparativa de preços venda sugerida ao publico, entre os diversos países em estudo.
The Asian and Pacific Centre for Transfer of Technology (APCTT) is a regional institution of the United Nations Economic and Social Commission for Asia and the Pacific (ESCAP) servicing the Asia-Pacific region.
The National Research Development Corporation (NRDC) was a non departmental government body established by the British Government to transfer technology from the public sector to the private sector.
TIFAC is an autonomous organization set up in 1988 under the Department of Science & Technology to look ahead in technology domain, assess the technology trajectories, and support innovation by networked actions in select areas of national importance.
Biotech Consortium India Limited (BCIL) is a public limited company, promoted by the Department of Biotechnology (DBT), Ministry of Science and Technology, Government of India and set up by All India Financial Institutions including IDBI, ICICI, IFCI, UTI and IFCI Venture Capital Funds Limited.
Objectives, scope, Organization and structure of retail and wholesale drug store, type and design, dispensing of proprietary products, legal requirements
Pilot plant Techniques and Product consideration for liquid dosage forms.D.R. Chandravanshi
CONTENTS:-
DEFINITION
INTRODUCTION
OBJECTIVES
LIQUID DOSAGE FORM
STEPS INVOLVED IN PILOT PLANT FOR ORAL LIQUID
GENERAL CONSIDERATION
Reporting responsibility
Personal requirements
Space requirements
Review of formula
Raw materials
Relevant processing equipments
Process evaluation
GMP consideration
Assurance
PILOT PLANT SCALE UP FOR SUSPENSION
PILOT PLANT SCALE UP FOR EMULSION
REFERENCES
A platform is a group of technologies that are used as a base
or infrastructure upon which other applications, technologies
or processes are developed for the end-user.
“a common or standard method, equipment, procedure or work practice that may be applied to the research, development or manufacturing of different products ” An array of multi-disciplinary technologies covering major aspects of the drug discovery and development processes have been established in Institute of Biotechnology and Pharmaceutical Research (IBPR)
Technology Transfer Related Documents.pptxAfroj Shaikh
SlideShare Description: Technology Transfer Related Documents
Welcome to SlideShare's collection of technology transfer related documents in the field of pharmacy. This presentation focuses on the essential documentation needed for successful technology transfer in pharmaceutical manufacturing, emphasizing its role in ensuring quality, safety, and regulatory compliance.
Technology transfer plays a crucial role in the dynamic and ever-evolving field of pharmacy. It facilitates the smooth transfer of knowledge, processes, and technologies from research and development to commercial production. To ensure a seamless transition, a well-defined set of documents is required to capture critical information, procedures, and controls.
This SlideShare presentation explores the key documents involved in technology transfer within the pharmaceutical industry. The technology transfer protocol is discussed first, highlighting its purpose, contents, and significance. Acting as a roadmap, this protocol outlines the transfer scope, stakeholder responsibilities, timelines, and acceptance criteria, promoting effective communication and collaboration between the sending and receiving units.
The importance of comprehensive process descriptions is also emphasized. These documents detail the manufacturing process, equipment specifications, critical parameters, and in-process controls. They serve as a guide for the receiving unit to replicate the process accurately, ensuring consistent product quality and performance.
Validation and qualification protocols are addressed as well, highlighting their role in verifying that equipment, processes, and systems are suitable for their intended use. These protocols are crucial for meeting regulatory requirements and mitigating risks associated with the transfer.
Analytical method transfer documents are discussed next, encompassing the procedures for transferring and validating analytical methods used to assess the quality attributes of pharmaceutical products. Robust analytical methods are essential to ensure accurate and reliable test results throughout the product lifecycle.
The presentation also covers documentation related to training, risk assessments, change control, and deviation management. These documents help establish a robust quality management system, ensuring adherence to regulatory standards and facilitating continuous improvement.
Whether you're involved in technology transfer, quality assurance, or regulatory affairs, this SlideShare is a valuable resource for understanding the essential documents involved in successful technology transfer within the pharmaceutical industry. By leveraging these documents effectively, you can ensure a seamless transfer process, maintain product quality, and uphold patient safety.
Explore our SlideShare and gain the knowledge necessary to navigate the intricacies of technology transfer in pharmacy. Stay updated with the latest best practices and regulatory guidelines.
A pharmacist is the person of drugs or the expert on drugs. He is the only expert on drugs, for expertise regarding drugs requires knowledge in depth in all the facts of pharmacy. It is her professional responsibility to know all about the drugs. No educational program other than that in pharmacy provides the background to understand completely all about drugs.
Among the professions of pharmacists like community pharmacy, institutional pharmacy, whole sale pharmacy, industrial pharmacy, government service, pharmaceutical education, organizational management, in my country industrial pharmacy offers great opportunity to the pharmacists.
Industrial pharmacy is a profession of unique hybrid of business and profession.
So an industrial pharmacist should have proper knowledge about drugs and also about medical progress, commence marketing and technology. To be a self-sufficient pharmacist beside academic knowledge, practical knowledge is essential.
This is why after appearing the Bachelor of Pharmacy examination in-plant training was arranged by the department in renowned pharmaceuticals industries. This training has sharpened my academic knowledge what I learnt in the last four years .I have completed my training in Popular Pharmaceuticals Limited a fast growing pharmaceutical company in Bangladesh.
COPP/CPP it certification of pharmaceutical product for reviewing QSE i.e. Quality, Sefty,Efficacy of product. it important certification for exporting it may required by importing country.
O presente documento, GUIA REGULATORIO, visa mostrar o caminho regulatório – 2016, necessário a ser cumprido por entidades para exportação de produtos Farmacêuticos – Medicamentos, ao Peru.
Em cada slide encontram-se as informações para cada instancia no cumprimento de normativas peruanas, com links internos (hiperlinks) para abrir os documentos originais. Não todo está traduzido ao português, mas a intenção é justamente poder ter ao alcance de um simples click ou leitura compreensiva, e em forma organizada o estritamente necessário em termos legais para compor o dossiê do produto.
Arquivos contidos no paquete:
Documento principal em Power Point;
Normativas inerentes ao processo;
Documentos complementares;
Esta mesma modalidade de apresentação dinâmica pode ser extensivo para outros produtos (Biológicos, Homeopáticos, Fitoterápicos, Cosméticos, Alimentos, etc.).
Acompanha treinamento presencial ou virtual para um entendimento aprofundado de como empregar o mesmo, caso assim seja solicitado.
Este trabalho pode estar disponível, além do idioma Português, nos idiomas de Espanhol e Inglês.
Na mesma modalidade de apresentação estão disposto outros países como Argentina, Colômbia e Chile.
Para os demais países da América Latina, este trabalho se faz sobre encomenda.
Por solicitação, pode ser realizado comparativa de preços venda sugerida ao publico, entre os diversos países em estudo.
Medicated Chewing Gum (MCG) is a novel drug delivery system containing masticatory gum base with pharmacologically active ingredient and intended to use for local treatment of mouth diseases or systemic absorption through oral mucosa.
1. Muchos de los que insisten en poner fechas al fin del mundo y un inminente apocalipsis lo hacen para lucrar con la fe de gente sincera vemos aquí un repaso través de la historia a personajes, que aprovechándose del miedo la curiosidad o fascinación por el fin, venden más libros, revistas folletos, etc
Alegem să participăm! Buletin informativ al Clubului pentru Cetățenie Activă ...Moldova Europeană
Alegem să participăm! Buletin informativ al Clubului pentru Cetățenie Activă din or. Căușeni, Nr. 5
Clubul pentru Cetățenie Activă din or. Căușeni, a publicat a cincea ediție a Buletinului informativ ”Alegem să participăm!”,
Based on Industrial Training internship report in B pharmacy 4th year.
At Roseate Medicare Pharmaceutical Industry Solan.
From Shanti Niketan college of Pharmacy (Malther ,Ratti ,Mandi ,HP 175008)
INDUSTRIAL TRAINING REPORT (B-pharmacy ) Zentiva pharmaceutical industry PrakashKumar721
Location:- GIDC Estate Ankleswar
393002, Dist. Bharuch ,Gujrat India
Zentiva is a producer of high-quality affordable medicines serving patients in Europe and beyond. With a dedicated team of more than 4,700 people and a network of production sites - including flagship sites in Prague, Bucharest and Ankleshwar - Zentiva strives to be the champion of branded and generic medicines in Europe to better supportpeople’s daily healthcare needs. At Zentiva it is our aspiration that healthcare should be a right and not a privilege. More than ever, people need better access to high quality affordable medicines and healthcare. We work in partnership with physicians, pharmacists, wholesalers, regulators and governments to provide the everyday solutions that we all depend on.
About Zentiva’s Ankleshwar site
Established in 1987, the Ankleshwar manufacturing site has a chemistry and biotechnology development center, and manufactures both intermediates and pharmaceutical formulations. A large producer of tablets, the Ankleshwar site manufactures more than 6 billion tablets annually.
Mission &Values:-
Zentiva is a leading developer and supplier of high-quality affordable prescription medicines and consumer brands. As Zentiva grows more people get the medicine they need. Our business is built on trust and responsibility with the patient at the heart of everything we do. Zentiva has established 6 shared SuperpowerZ which frame the values and behaviours we expect of our team and how we will build a healthy business that we can all be proud of.
TABLET-SECTION
Tablet:-
A tablet is a mixture of active substances and excipients, usually in powder form, pressed or compacted into a solid. The excipients include binders, Glidants (flow aids) and lubricants to ensure efficient tabletting, disintegrates to ensure that the tablet breaks up in the digestive tract; sweeteners or flavors to mask the taste of bad-tasting active ingredients; and pigments to make uncoated tablets visually attractive. A coating may be applied to hide the taste of the tablet's components, to make the tablet smoother and easier to swallow, and to make it more resistant to the environment, extending its shelf life.
Advantage
• Production aspect
Large scale production at lowest cost
Easiest and cheapest to package and ship
High stability
• User aspect (doctor, pharmacist, patient)
Easy to handling.
Lightest and most compact.
Greatest dose precision & least content variability.
Coating can mark unpleasant tastes & improve pt. acceptability.
PHARMACEUTICAL PRODUCT BY ZENTIVA PHARMACEUTICAL PVT.LTD:-
1. Avil -25 mg
2. Trental-400
3. Paracetamol-500mg
4. Ramilich-( 5, 25mg)
5. Ramipril-25mg
6. Zuglimate-500mg
7. Clopidogrel-75mg
8. Metformin-100mg
QUALITY CONTROL AND QUALITY ASSUARANCE
Quality control is the part of GMP that deals with sampling, specification, and testing, as well as organisation, documentation, and release procedures to ensure that necessary and
Incepta pharmaceutical Ltd. is one of the leading pharmaceutical company in Bangladesh. They provide their best effort to produce a quality product. They have modern and sophisticated machinery and all facility required to comply with the GMP.
My internship was at Amr Dairy, Amreli . During my internship I had been rotated different departments as storage, production, utility, ETP, CIP, packing, transportation etc in two weeks, this movement and working provide a complete knowledge of Dairy production.
Good Manufacturing Practice is a set of regulations, codes, and guidelines for the manufacture of drug substances and drug products, medical devices, in vivo and in vitro diagnostic products, and foods.
A detailed study of Transition Metal Complexes of a Schiff base with its Phys...Abhishek Ghara
The many activities of metal ions in biology have stimulated the development of metal based therapeutics. It has been found that biologically active compounds become more effective and bacteriostatic upon chelation with metal ions also the biological activity of many drugs has been shown to be enhanced on complexing with metal ions, hence promoting their use in Pharmacology. The present work deals with the synthesis of metal complexes derived from a novel Schiff base drug synthesized from urea and salicylaldehyde and its physico-chemical analysis to find out ligand- metal ratio of this complex in solution. For the structure elucidation of these complexes “Monovariation method (Mole ratio method/ Yoe-Jones Method)” has been used to ascertain the ligand-metal ratio in the complex. The stability constant of the formed complex was calculated by molar conductance measurement using Modified Job’s method (Method of Continuous Variations). The analysis has been carried out using conductometry. To confirm metal-ligand ratio, conductometric titrations were carried out at room temperature using analytical grade metal salts. Titrations were carried out with “systronics conductivity-meter” using dip type conductivity cell having cell constant 1 at room temperature.
3. ACKNOWLEDGEMENT
I am thankful to the Quality Assurance Manager Mr. Sudip Ganguly of
Gluconate Health Limited because without his approval I could not join and
complete my training.
I am also thankful to Works Manager, Production Manager, Quality Control
Manager and all other Chemist and Workers for their generous co-operation.
I am greatly thankful to Dr. Arnab Samanta (Principal of NSCBIP) and Dr.
Sudipa Das (Assistant Professor of NSCBIP) for giving me a chance to perform the
industrial training.
Last but not least my special thanks to the most important persons of my
life, my Parents for their never ending support & blessings.
4. CONTENT
1. Company Profile (1)
2. Layout of Industry (2)
3. Organizational Structure (3)
4. List of Raw Material (4)
5. Production Department (5-15)
Instrument
Mfg. Process
6. Q.C. Department (16)
7. Packaging Department (17)
8. Store Department (18)
9. List of Product Name (Generic) (19)
10. Good Manufacturing Process (20)
11. Conclusion (21)
5. COMPANY PROFILE
Gluconate Health Ltd. factory Is situated in the Dumdum Cantonment,
Health Institute Road and the registered head office is 2, Durga Charan Doctor
Lane, Kolkata- 700014, West Bengal.
The 1st. Chief Minister of West Bengal and the great visionary Dr.Bidhan
Chandra Roy’s effort to discover anti malarial drug from ‘Chhatim’ tree (Astonia
Scolaris), culminated to the foundation of the pharmaceutical manufacturing
company Gluconate India Limited in 1933. Following this in 1936 some young
ambitious medical practitioners formed Indian Health Institute Ltd, to
manufacture Vaccine, Injections, Tablets, Capsules and liquids. Gluconate India
Limited and Indian Health Ph. Ltd. were merged and in 1990 Gluconate Health
Limited were formed on the principle of ‘having best of both’.
Since 1987 both these companies have been nationalized and presently
Gluconate Health Limited is a wholly owned enterprise under Government of
West Bengal, which contrary to the popular belief about government run
companies are likely to be unhealthy, GHL stands out proudly and have shown
steady growth and profit with promise to grow high in coming years. We have
always extended our active effort to ensure the success of any healthcare
program taken by the government at any level and our commitment towards this
are always on priority. We are a major player in the country in supplying essential
medicines at most affordable price to various government bodies. We have
achieved commendable success by supplying our high quality medicines to ensure
the success of “women and child development program” under UNDP.
We supply a large number of our products in high quantity to Govt. of
W.Bengal, Bihar, Jharkhand, Chhattisgarh, Tripura, Andhra Pradesh, PGI
Chandigarh, ICDS, various Government of India healthcare program and many
more reputed institutions.
1
18. Bottle Labelling Machine
MANUFACTURING PROCESS OF LIQUID PREPARATION
14
19. After sealing and labelling the bottle will be packed in large cartoon box.
100 bottles in one box are packed, sealed and stored for marketing
requirements.
15
20. QUALITY CONTROL DEPARTMENT
INSTRUMENT AVAILABLE:
1. PH
meter
2. Conductivity meter
3. Leak test apparatus
4. Polarimeter
5. Fribilator USP
6. Melting point apparatus
7. Hot air oven
8. DV-E viscometer
9. Mechanical stirrer
10.Dissolution tester USP
11.Media preparator
12.Digital weighing machine
13.Disintegration test appratus
14.Spectophotometric meter
QUALITY TEST (Norfloxacin tablet):
TITRATION (NON-AQUEOUS):
Tablet triturate 50ml Glacial acetic acid Produce raddish colour
Add Perchloric acid (0.1M) dropwise Produce ash colour.
DISSOLUTION TEST:
Six tablets give in dissolution test apparatus for 30 minutes at 50
rpm.
Filter the tablet solution in six measuring cylinder (in each 20ml).
Take 1ml tablet solution in each and transfer in different volumetric
flask (six) and fillup the volume upto 100ml by acetic buffer.
16
21. PACKAGING
BLISTER PACKING
(For Tablets and Capsules)
It is formed in PVC sheet and tablets are packed using Aluminium foil on opposite
side. Sealed in normal Blister pack machine is used.
Formation Roller
Formation Heater
Hopper
Bowl Dish
Channel
Printer
Cutter
Then the strips are checked and collected and 10 tablet strips are packed into a
small box and then 100 small boxes are packed in a large box and sealed for
marketing requirements.
A strip contains 10 or 20 tablets depending upon the size & shape of the tablet.
h
17
22. STORE
In the store of the industry raw materials are stored for the manufacturing and
production. It has four zones, first quqrantine for primary uploading point, second
is the red zone where rejected materials are stored, third is the green zone where
quality control test passed materials are stored and the last one yellow zone
where primary rejected materials are stored.
18
23. LIST OF PRODUCT
TABLETS
SL. NO. NAME OF THE PRODUCT PKG DESCRIPTION
1
2
3
4
5
6
Azethromycin 500mg
Norfloxacin 400mg
Paracetamol 500mg
Ibuprofen 200mg + 400mg
Metronidazole 200mg +
400mg
Ranitidine 150mg
10*10’s
10*10’s
10*10’s
10*10’s
10*10’s
10*10’s
Anti-biotic
Anti-microbial
Antipyretic
Anti Inflammatory
Anti Amoebic
Anti ulcer
CAPSULES
SL. NO. NAME OF THE PRODUCT PKG DESCRIPTION
1
2
3
4
Amoxycillin 250mg
Ciprofloxacin 250mg + 500mg
Ampicillin + Cloxacillin 250mg
Rifampicin 450mg
10*10’s
10*10’s
10*10’s
10*10’s
Antibiotic
Anti-microbial
Antibiotic
Anti-T.B.
LIQUIDS
SL. NO. NAME OF THE PRODUCT PKG DESCRIPTION
1
2
3
4
5
6
7
8
9
Metronidazole suspension
Paracetamol syrup
Syrup Molar Sodium Lactate
Gention Violet
Erythromycin Suspension
Alkacitron
Glucorex
Zymoton
B com T
60ml
60ml
450ml
100ml
60ml
100ml
100ml
100ml
200ml
Amoebicidal
Antipyretic
Oxidant
Dermatological Agent
Anti-microbial Agent
Urinary Infection
Expectorant
Digestive enzyme secretion
Vit B
19
24. CONCLUSION
It has been a pleasure to undergo training GLUCONATE HEALTH LTD organization;
GLUCONATE HEALTH LTD is real boost for the economic development in the
countries, India. Responsible authorities should be more flexible in promotion of
such organization creating employment and effective utilization of locally
available resources.
Observing the various instruments used in different sections give me the much
needed exposure to the pharma industry. All these aspects are really learnable
area where one can gather a lot of knowledge.
The adoption and maintainance of the quality policy are readily astonishing and
the purpose is very clear, effective and praise worthy.
Our training programmed was assisted by the helping hands of the employees of
this organization is thus a fullfillment of our objectives and the learning will
obviously be an asset for us in the long future.
21