Africa pharmaceutical market, industry analysis, forecast 2024aarktech2018
The report covers the present ground scenario and the future growth prospects of Africa Pharmaceuticals Market. Furthermore, it includes statistics of Branded and Generic Drugs along with the details of ongoing projects in the pharma sector in Africa.
East African Pharmaceutical Sector: Opportunities and ChallengesPharmaAfrica
Presentation by Nazeem Mohamed, Federation of East African Pharmaceutical Manufacturers made at the Euro-Africa Health Investment Conference, March 26 - 27, 2013, London, United Kingdom.
Opportunities & Challenges in West Africa's (Ghana & Nigeria) Healthcare and ...Aiswariya Chidambaram
This presentation made at the Pharma Insights Briefing session of CPhI Worldwide 2014, Paris, provides information on the market opportunities of
the fastest growing pharmaceutical markets in Africa: Ghana and Nigeria.
• Market sizing and Growth Trends
• Key Merger, Acquisition and Partnership Assessment
• Market Drivers and Challenges
• Pharmaceutical Procurement, Supply, Distribution and Retail
• SWOT and PESTLE Analysis
• Competitive Landscape Analysis
• Therapeutic Area Growth Analysis
• Strategic Recommendations
Africa pharmaceutical market, industry analysis, forecast 2024aarktech2018
The report covers the present ground scenario and the future growth prospects of Africa Pharmaceuticals Market. Furthermore, it includes statistics of Branded and Generic Drugs along with the details of ongoing projects in the pharma sector in Africa.
East African Pharmaceutical Sector: Opportunities and ChallengesPharmaAfrica
Presentation by Nazeem Mohamed, Federation of East African Pharmaceutical Manufacturers made at the Euro-Africa Health Investment Conference, March 26 - 27, 2013, London, United Kingdom.
Opportunities & Challenges in West Africa's (Ghana & Nigeria) Healthcare and ...Aiswariya Chidambaram
This presentation made at the Pharma Insights Briefing session of CPhI Worldwide 2014, Paris, provides information on the market opportunities of
the fastest growing pharmaceutical markets in Africa: Ghana and Nigeria.
• Market sizing and Growth Trends
• Key Merger, Acquisition and Partnership Assessment
• Market Drivers and Challenges
• Pharmaceutical Procurement, Supply, Distribution and Retail
• SWOT and PESTLE Analysis
• Competitive Landscape Analysis
• Therapeutic Area Growth Analysis
• Strategic Recommendations
Presentation by NEPAD Agency on the African Medicines Regulatory Harmonisation made at the Euro-Africa Health Investment Conference, March 26 - 27, 2013, London, United Kingdom.
Presentation by Adil Zanfari, President, Genpharma, Morocco made at the Euro-Africa Health Investment Conference, March 26 - 27, 2013, London, United Kingdom.
China Pharmaceutical Market : SWOT Analysis, Government policies, Business an...Maria Robert
Purchase a copy of this report @ http://www.lifescienceindustryresearch.com/purchase?rname=17129.
Pharmaceutical Industry in China – Cutting-Edge Analysis of Multinational and Chinese Pharma Companies, Industry Trends, Environment, Regulation, Market Drivers, Restraints, Opportunities & Challenges report presented by Company (e.g., AMOYTOP BIOTECH, BEIJING CONTINENT PHARMACEUTICALS, FUSOGEN, SHANGHAI HUAGUAN BIOCHIP, SIBIONO GENETECH, ABBOTT, ROCHE, PFIZER, GSK, NOVARTIS) & by Therapeutic Area (e.g., Anti-infective, Cancer, Diabetes, Dementia, Depression)
Indian Pharmaceutical Export Market - Top Export Destinations for Indian Phar...Irish Pereira
By Mr. Irish Pereira. The report present snapshot of Indian Pharmaceutical industry in both domestic as well as export market. It is collation of facts pertaining to Indian pharma exports and explore key emerging trends pertaining to pharma export market. It describes key players of Indian pharma market and their export orientation as in their target export destinations, their focus therapies etc.
Fact sheet:
1) Indian Pharma Market size 2015
2) Indian pharmaceutical market segments by value
3)Patented (Innovator) Vs Generics Scenario
4)Growth drivers of Indian pharmaceutical industry
5) Indian Pharmaceutical sector – SWOT Analysis
6)PHARMEXCIL – Facilitating agency for Indian Pharma Exports
7) Indian Pharmaceutical Exports (USD bn)
8)Formulations share in Total Pharma Exports (2014-15)
9) Top 25 destination countries of India’s pharmaceutical exports during 2013-14 (INR mn)
10) Major Indian Pharma Companies (By Revenue-USD mn)
11) Pharma players and their export destinations
Sun Pharma,Dr. Reddy’s Lab,
CIPLA, Lupin, Aurobindo, Cadila Healthcare, Torrent Pharma, Wockhardt,
12) Emerging trends in Indian Pharma Market
Key success factors to win in MENA pharmaceutical market, Market access planning, creating value, major challenges and changes in Pharmaceutical culture in MENA
Strategic Analysis of the Indian Pharmaceutical Contract Manufacturing Market...Aiswariya Chidambaram
The Indian Pharmaceutical CMO market has been analyzed and assessed with respect to APIs and finished dose formulations (solids, liquids and injectables). Strategic recommendations for the success of market participants have been provided.
Introduction Indian Pharmaceutical market, SWOT analysis, PEST Analysis, Timeline analysis of Sun Pharma, Glaxo Smith Kline, Mankind, CIPLA and Zydus Cadila.
Presentation by NEPAD Agency on the African Medicines Regulatory Harmonisation made at the Euro-Africa Health Investment Conference, March 26 - 27, 2013, London, United Kingdom.
Presentation by Adil Zanfari, President, Genpharma, Morocco made at the Euro-Africa Health Investment Conference, March 26 - 27, 2013, London, United Kingdom.
China Pharmaceutical Market : SWOT Analysis, Government policies, Business an...Maria Robert
Purchase a copy of this report @ http://www.lifescienceindustryresearch.com/purchase?rname=17129.
Pharmaceutical Industry in China – Cutting-Edge Analysis of Multinational and Chinese Pharma Companies, Industry Trends, Environment, Regulation, Market Drivers, Restraints, Opportunities & Challenges report presented by Company (e.g., AMOYTOP BIOTECH, BEIJING CONTINENT PHARMACEUTICALS, FUSOGEN, SHANGHAI HUAGUAN BIOCHIP, SIBIONO GENETECH, ABBOTT, ROCHE, PFIZER, GSK, NOVARTIS) & by Therapeutic Area (e.g., Anti-infective, Cancer, Diabetes, Dementia, Depression)
Indian Pharmaceutical Export Market - Top Export Destinations for Indian Phar...Irish Pereira
By Mr. Irish Pereira. The report present snapshot of Indian Pharmaceutical industry in both domestic as well as export market. It is collation of facts pertaining to Indian pharma exports and explore key emerging trends pertaining to pharma export market. It describes key players of Indian pharma market and their export orientation as in their target export destinations, their focus therapies etc.
Fact sheet:
1) Indian Pharma Market size 2015
2) Indian pharmaceutical market segments by value
3)Patented (Innovator) Vs Generics Scenario
4)Growth drivers of Indian pharmaceutical industry
5) Indian Pharmaceutical sector – SWOT Analysis
6)PHARMEXCIL – Facilitating agency for Indian Pharma Exports
7) Indian Pharmaceutical Exports (USD bn)
8)Formulations share in Total Pharma Exports (2014-15)
9) Top 25 destination countries of India’s pharmaceutical exports during 2013-14 (INR mn)
10) Major Indian Pharma Companies (By Revenue-USD mn)
11) Pharma players and their export destinations
Sun Pharma,Dr. Reddy’s Lab,
CIPLA, Lupin, Aurobindo, Cadila Healthcare, Torrent Pharma, Wockhardt,
12) Emerging trends in Indian Pharma Market
Key success factors to win in MENA pharmaceutical market, Market access planning, creating value, major challenges and changes in Pharmaceutical culture in MENA
Strategic Analysis of the Indian Pharmaceutical Contract Manufacturing Market...Aiswariya Chidambaram
The Indian Pharmaceutical CMO market has been analyzed and assessed with respect to APIs and finished dose formulations (solids, liquids and injectables). Strategic recommendations for the success of market participants have been provided.
Introduction Indian Pharmaceutical market, SWOT analysis, PEST Analysis, Timeline analysis of Sun Pharma, Glaxo Smith Kline, Mankind, CIPLA and Zydus Cadila.
What is the "Drugs (Prices Control) Order (DPCO)" ? The Drugs Prices Control Order, 1995 is an order issued by the Government of India under Sec. 3 of Essential Commodities Act, 1955 to regulate the prices of drugs.
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Polyhydroxyalkanoate are linear polyesters that are produced from fermentation of lipid or sugar by bacteria. The rising demand for biodegradable materials, increase in oil prices and policies concerning green procurement are the driving factors for investment by companies in this market.
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Cultivating and maintaining discipline within teams is a critical differentiator for successful organisations.
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A Memorandum of Association (MOA) is a legal document that outlines the fundamental principles and objectives upon which a company operates. It serves as the company's charter or constitution and defines the scope of its activities. Here's a detailed note on the MOA:
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Name Clause: This clause states the name of the company, which should end with words like "Limited" or "Ltd." for a public limited company and "Private Limited" or "Pvt. Ltd." for a private limited company.
https://seribangash.com/article-of-association-is-legal-doc-of-company/
Registered Office Clause: It specifies the location where the company's registered office is situated. This office is where all official communications and notices are sent.
Objective Clause: This clause delineates the main objectives for which the company is formed. It's important to define these objectives clearly, as the company cannot undertake activities beyond those mentioned in this clause.
www.seribangash.com
Liability Clause: It outlines the extent of liability of the company's members. In the case of companies limited by shares, the liability of members is limited to the amount unpaid on their shares. For companies limited by guarantee, members' liability is limited to the amount they undertake to contribute if the company is wound up.
https://seribangash.com/promotors-is-person-conceived-formation-company/
Capital Clause: This clause specifies the authorized capital of the company, i.e., the maximum amount of share capital the company is authorized to issue. It also mentions the division of this capital into shares and their respective nominal value.
Association Clause: It simply states that the subscribers wish to form a company and agree to become members of it, in accordance with the terms of the MOA.
Importance of Memorandum of Association:
Legal Requirement: The MOA is a legal requirement for the formation of a company. It must be filed with the Registrar of Companies during the incorporation process.
Constitutional Document: It serves as the company's constitutional document, defining its scope, powers, and limitations.
Protection of Members: It protects the interests of the company's members by clearly defining the objectives and limiting their liability.
External Communication: It provides clarity to external parties, such as investors, creditors, and regulatory authorities, regarding the company's objectives and powers.
https://seribangash.com/difference-public-and-private-company-law/
Binding Authority: The company and its members are bound by the provisions of the MOA. Any action taken beyond its scope may be considered ultra vires (beyond the powers) of the company and therefore void.
Amendment of MOA:
While the MOA lays down the company's fundamental principles, it is not entirely immutable. It can be amended, but only under specific circumstances and in compliance with legal procedures. Amendments typically require shareholder
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This 60-minute webinar, sponsored by Adobe, was delivered for the Training Mag Network. It explored the five elements of SPARK: Storytelling, Purpose, Action, Relationships, and Kudos. Knowing how to tell a well-structured story is key to building long-term memory. Stating a clear purpose that doesn't take away from the discovery learning process is critical. Ensuring that people move from theory to practical application is imperative. Creating strong social learning is the key to commitment and engagement. Validating and affirming participants' comments is the way to create a positive learning environment.
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Premium MEAN Stack Development Solutions for Modern BusinessesSynapseIndia
Stay ahead of the curve with our premium MEAN Stack Development Solutions. Our expert developers utilize MongoDB, Express.js, AngularJS, and Node.js to create modern and responsive web applications. Trust us for cutting-edge solutions that drive your business growth and success.
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Discover the innovative and creative projects that highlight my journey throu...dylandmeas
Discover the innovative and creative projects that highlight my journey through Full Sail University. Below, you’ll find a collection of my work showcasing my skills and expertise in digital marketing, event planning, and media production.
3.0 Project 2_ Developing My Brand Identity Kit.pptxtanyjahb
A personal brand exploration presentation summarizes an individual's unique qualities and goals, covering strengths, values, passions, and target audience. It helps individuals understand what makes them stand out, their desired image, and how they aim to achieve it.
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As an Army veteran dedicated to lifelong learning, I bring a disciplined, strategic mindset to my pursuits. I am constantly expanding my knowledge to innovate and lead effectively. My journey is driven by a commitment to excellence, and to make a meaningful impact in the world.
What is the TDS Return Filing Due Date for FY 2024-25.pdfseoforlegalpillers
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Implicitly or explicitly all competing businesses employ a strategy to select a mix
of marketing resources. Formulating such competitive strategies fundamentally
involves recognizing relationships between elements of the marketing mix (e.g.,
price and product quality), as well as assessing competitive and market conditions
(i.e., industry structure in the language of economics).
Indian pharmaceutical Industry - Committed to a healthier life
1. SHANKAR R 14114
GEORGE JACOB 14095
DIVYA LIZ GEORGE 14093
DHARA B SHAH 14067
MARY MONISHA 14060
G5
INDIAN PHARMACEUTICAL INDUSTRY
Committed to a healthier
life
2. Indian Pharmaceuticals
World’s 3rd largest [volume]
6th largest market globally [size]
2.4% of the Global Pharma Industry
Domestic demand [2014-15] close to $36.8 billion
cCAGR 13%, to continue for the next 5 years
90% of drugs sold estimated to be generics
1
3. KEY STRENGTHS
Fair protection of intellectual property rights
Strong manufacturing base.
Drug prices 1/10th of international price and 40 % cheaper to set up plants.
60-70% cheaper for bulk drug production.
Highly trained pool of scientists and professionals.
Highest quality approvals from USFDA
Growing biotechnology industry.
Low labour cost
2
14. Growth drivers
Demand Side
Drivers
Policy Support
Supply Side
Drivers
Cost advantage
Manufacturing hub
546 sites registered
Penetration of chemists
Accessibility to improve
Health insurance
Stress related disease
Diagnostic facilities
Reduction in approval
time
Pharma education
Accessibility for BPL
Exemptions
10
15. Key challenges
Drug Quality, not adhering to cGMP
Clinical trial quality
Low margin of profits due to Govt pricing policy – Drug price control order
Patent issues
Low input for R & D
USFDA checks
11
16. Opportunities
$44 billion lose due to patent expiry in US
Expansion of Biosimilars and Bio-pharmaceuticals.
Growth of CRAMS
NMITLI & DPRP schemes
Fiscal incentives to R &D units
12
17. India’s share in anda approvals
370
398
433
418 421
442
499
380 379
59
21%
28%
29% 30% 31%
35%
40%
43%
34%
41%
0%
5%
10%
15%
20%
25%
30%
35%
40%
45%
50%
0
100
200
300
400
500
600
2006 2007 2008 2009 2010 2011 2012 2013 2014 YTD 2015
Total Approvals India as a % of total approvals
13
18. BIOSIMILAR : THE next big thing
Active
Ingredients
sourced
from living
organisms
Sensitive to
storage and
handling
Approval –
Multi step
process
Complex
nature –
Not easily
copied
USD 1.4
billion by
2016
Overall
market
sales – 20%
growth
Cadila
Biocon
Dr Reddy’s
Lupin
WockhardtCadila’s
Exemptia,
biosilmilar
of Humira
14
3rd largest pharmaceuticals market by 2020.
20% of global exports in generics.
USD 45 Billion in revenue by 2020.
USD 26.1 Billion in generics by 2016.
USD 200 Billion to be spent on infrastructure by 2024.
49% of all drug master filings registered in the USA
The Drugs and Cosmetics Act, 1940 (Drugs Act) and Drugs and Cosmetic Rules, 1945 (Drug rules) regulate the
import, manufacture, distribution and sale of drugs in India. Under the provisions of these Acts, the Centre appoints
the Drugs Technical Advisory Board (DTAB) to advise the central government and the state governments on
technical matters.
The responsibility to enforce the Drugs Act is entrusted with both the central government and the respective state
governments. Under the Drugs and Cosmetics Act, state authorities are responsible for regulating the manufacturing,
sale and distribution of drugs, whereas the central authorities are responsible for approving new drugs and clinical
trials, laying down the standards for drugs, controlling the quality of imported drugs and coordinating
the activities of
state drug control organisations.
The Drugs Controller General of India (DCGI) is the central body that coordinates
the activities of state drug control
organisations, formulates policies and ensures uniform implementation of the Drugs Act throughout India. It is also
responsible for approval of licenses of specified categories of drugs, such as blood and blood products, IV Fluids,
Vaccine and Sera.
Indian pharmaceuticals industry is mainly regulated on the basis of patents, price and quality
Source: CRISIL
Patents
Before 2005, the regulatory system in India focused only on process patents. Indian pharmaceutical companies
thrived during the process patent regime. They would reengineer
products of global innovator companies, which were
unavailable in India, and launch them in the country as generics, as India did not recognise the product patents. In
this manner, Indian companies gained process chemistry skills, but did not focus on R&D for new drug discovery.
In January 2005, India complied with the World Trade Organisation (WTO) to follow the product patent regime [sale of
reengineered
products (for drugs patented after 1995) is restricted]. However, enterprises, which had made
significant investments and were producing and marketing the concerned product prior to January 1, 2005 and which
continue to manufacture the product covered by the patent on the date of grant of the patent, are protected, and the
patentee cannot institute infringement suits against them, but would be entitled to reasonable royalty.
For a detailed analysis on the product patent regime and its impact, please refer to the Thematic Coverage section.
Drug prices
The Drug Price Control Order (DPCO) fixes the ceiling price of some APIs and formulations. APIs and formulations
falling under the purview of the legislation are called scheduled drugs and scheduled formulations. The National
Pharmaceutical Pricing Authority (NPPA) collects data and studies the pricing structure of APIs and formulations and accordingly makes recommendations to the Ministry of Chemicals and Fertilisers.
The new Pharmaceutical Policy, notified in 2012, intends to bring 348 essential drugs in the National List of Essential
Medicines (NLEM), under the purview of the DPCO. With this policy, the market size of drugs under price control will
increase from 1520
per cent of the domestic formulations market to 2030
per cent. The policy also introduces a
radical change in the mechanism of control: shifting from the current costbased
control to a marketbased
price
mechanism.
Under the policy, the ceiling price for each drug under control would be fixed as the simple average price of brands
having more than 1 per cent market share (by value) in the sales (MAT Moving
Annual Turnover) of that particular
molecule. Thus, prices of brands which are higher than this ceiling will need to be lowered. The ceiling prices will be
allowed an annual increase as per the Wholesale Price Index (WPI). Prices will be recalculated using MAT only once
in five years or when the NLEM is updated.
Price of drugs that were part of the earlier policy, but do not come under the current policy, would be frozen for a year
and, thereafter, allowed a maximum annual increase of 10 per cent. A 10 per cent increase would also be the limit for
prices of drugs outside the government's price control.
Quality
No drug can be imported, manufactured, stocked, sold or distributed in India unless it meets the quality standards
laid down in the Drugs Act. All companies have to comply with Schedule M of the Act, which outlines various
requirements for manufacturing drugs and pharmaceuticals by applying cGMP (current Good Manufacturing Practice).
cGMP has to be followed for control and management of manufacturing and quality control testing of drugs.