✓ We are a Corporate Compliance organization having our presence across the globe aiming to ease compliance
and assist in business evolution.
✓ We ensure that your business is up to pace with todays hyper-dynamic corporate legal structure(s)
✓ We take care of your compliance, so you can focus on your business.
✓ We are a corporate compliance organisation with expertise at providing pollution related and waste
management advisory.
✓ We have facilitated more 5000+ clients in attainment of there business licences and registrations and more than
300 clients in obtaining there Ayush Manufacturing Licences throughout India.
A simple and essential guide to obtain a drug manufacturing license for ayurvedic medicine. It covers procedure, minimum requirements, documents & affidavits and all other necessities.
The use of herbal drugs for the prevention and treatment of various health ailments has been in practice from time immemorial. Generally it is believed that the risk associated with herbal drugs is very less, but reports on serious reactions are indicating to the need for development of effective marker systems for isolation and identification of the individual components.Standards for herbal drugs are being developed worldwide but as yet there is no common consensus as to how these should be adopted. Standardization, stability and quality control for herbal drugs are feasible, but difficult to accomplish. Further, the regulation of these drugs is not uniform across countries. There are variations in the methods used across medicine systems and countries in achieving stability and quality control. The present study attempts to identify the evolution of technical standards in manufacturing and the regulatory guideline development for commercialization of herbal drugs.
Keywords: survey was conducted to obtain primary data on challenges faced during production, commercialization, and marketing approval for traditional or herbal drugs in India and abroad. Responses were collected from companies by email, telephone, and in-person interviews and were analyzed to draw appropriate conclusions.The use of plants, parts of plants and isolated phytochemicals for the prevention and treatment of various health ailments has been in practice from time immemorial. It is estimated that about 25% of the drugs prescribed worldwide are derived from plants and 121 such active compounds are in use. Of the total 252 drugs in WHO's essential medicine list, 11% is exclusively of plant origin The use of plants, parts of plants and isolated phytochemicals for the prevention and treatment of various health ailments has been in practice from time immemorial. It is estimated that about 25% of the drugs prescribed worldwide are derived from plants and 121 such active compounds are in use. Of the total 252 drugs in WHO's essential medicine list, 11% is exclusively of plant origin .
Introduction Central Drug Testing Laboratories & Responsibilities
Role of Central Drugs Testing Laboratory
No of laboratories in India, No of laboratories in each State
Presented by
J. Vinay Krishna
Department of Industrial Pharmacy
A simple and essential guide to obtain a drug manufacturing license for ayurvedic medicine. It covers procedure, minimum requirements, documents & affidavits and all other necessities.
The use of herbal drugs for the prevention and treatment of various health ailments has been in practice from time immemorial. Generally it is believed that the risk associated with herbal drugs is very less, but reports on serious reactions are indicating to the need for development of effective marker systems for isolation and identification of the individual components.Standards for herbal drugs are being developed worldwide but as yet there is no common consensus as to how these should be adopted. Standardization, stability and quality control for herbal drugs are feasible, but difficult to accomplish. Further, the regulation of these drugs is not uniform across countries. There are variations in the methods used across medicine systems and countries in achieving stability and quality control. The present study attempts to identify the evolution of technical standards in manufacturing and the regulatory guideline development for commercialization of herbal drugs.
Keywords: survey was conducted to obtain primary data on challenges faced during production, commercialization, and marketing approval for traditional or herbal drugs in India and abroad. Responses were collected from companies by email, telephone, and in-person interviews and were analyzed to draw appropriate conclusions.The use of plants, parts of plants and isolated phytochemicals for the prevention and treatment of various health ailments has been in practice from time immemorial. It is estimated that about 25% of the drugs prescribed worldwide are derived from plants and 121 such active compounds are in use. Of the total 252 drugs in WHO's essential medicine list, 11% is exclusively of plant origin The use of plants, parts of plants and isolated phytochemicals for the prevention and treatment of various health ailments has been in practice from time immemorial. It is estimated that about 25% of the drugs prescribed worldwide are derived from plants and 121 such active compounds are in use. Of the total 252 drugs in WHO's essential medicine list, 11% is exclusively of plant origin .
Introduction Central Drug Testing Laboratories & Responsibilities
Role of Central Drugs Testing Laboratory
No of laboratories in India, No of laboratories in each State
Presented by
J. Vinay Krishna
Department of Industrial Pharmacy
The Drugs and Cosmetics Act, 1940 is an Act of the Parliament of India which regulates the import, manufacture and distribution of drugs in India. The primary objective of the act is to ensure that the drugs and cosmetics sold in India are safe, effective and conform to state quality standards.
This presentation is all about generic medicines.How it works in India its benefits and how one can make people aware about by the usage of these instead of branded ones.
A presentation aimed at providing information with regards to the Pharmacy Act, 1948.
-INTRODUCTION
-HISTORY OF THE ACT
-PHARMACY COUNCIL OF INDIA
-STATE PHARMACY COUNCIL
-SPECIAL PROVISIONS OF THE ACT
-OFFENCES AND PENALTIES
-CONCLUSION
-REFERENCES
Regulatory and industry requirements for botanical products, Prof. Dr. Basavaraj K. Nanjwade, KLE University College of Pharmacy, Belgavi/Belgaum, Karnataka, India.
This slide contains what is generic drug, what is advantages & disadvantages,reason behind unpopularity of generic drug in India, why generic drugs are important in India, why there is a need of generic drug policy, who are the regulatory authority, what are the act & laws, what policy existing in India for generic drug then Conclusion.
Regulatory requirements for herbal medicines: Herbal medicines are different from other types of medicines. The approval process is also different from other medicines. AYUSH Ministry given guidelines for approval of herbal medicines.
Query Solved
1. Regulatory requirements for herbal medicines
2. Herbal Medicines ke liye regulatory requirements
3. AYUSH ka important role in Herbal medicines launch
4. D and C act role in Herbal medicines
5. What are important steps to launch herbal medicines
Ease of doing business led India to become a more popular destination for the establishment of the
business. Numerous domestic and foreign entrepreneurs are exploring various avenues for establishing
their companies. This process involves a great deal of investment not only in terms of time, resources and
expertise but also in the procurement of necessary licenses and permits at the federal, state and
municipal levels.
Bio-medical Waste (Management & Handling) Rules, 1998 have defined Bio-Medical as a type of bio-waste because of the possibility
that it might contain hold bodily fluids like blood or other contaminants prescribed thereunder. These rules were prescribed by the
Ministry of Environment & Forests (MoEF) which was formed under the Environment (Protection) Act, 1986.
The Drugs and Cosmetics Act, 1940 is an Act of the Parliament of India which regulates the import, manufacture and distribution of drugs in India. The primary objective of the act is to ensure that the drugs and cosmetics sold in India are safe, effective and conform to state quality standards.
This presentation is all about generic medicines.How it works in India its benefits and how one can make people aware about by the usage of these instead of branded ones.
A presentation aimed at providing information with regards to the Pharmacy Act, 1948.
-INTRODUCTION
-HISTORY OF THE ACT
-PHARMACY COUNCIL OF INDIA
-STATE PHARMACY COUNCIL
-SPECIAL PROVISIONS OF THE ACT
-OFFENCES AND PENALTIES
-CONCLUSION
-REFERENCES
Regulatory and industry requirements for botanical products, Prof. Dr. Basavaraj K. Nanjwade, KLE University College of Pharmacy, Belgavi/Belgaum, Karnataka, India.
This slide contains what is generic drug, what is advantages & disadvantages,reason behind unpopularity of generic drug in India, why generic drugs are important in India, why there is a need of generic drug policy, who are the regulatory authority, what are the act & laws, what policy existing in India for generic drug then Conclusion.
Regulatory requirements for herbal medicines: Herbal medicines are different from other types of medicines. The approval process is also different from other medicines. AYUSH Ministry given guidelines for approval of herbal medicines.
Query Solved
1. Regulatory requirements for herbal medicines
2. Herbal Medicines ke liye regulatory requirements
3. AYUSH ka important role in Herbal medicines launch
4. D and C act role in Herbal medicines
5. What are important steps to launch herbal medicines
Ease of doing business led India to become a more popular destination for the establishment of the
business. Numerous domestic and foreign entrepreneurs are exploring various avenues for establishing
their companies. This process involves a great deal of investment not only in terms of time, resources and
expertise but also in the procurement of necessary licenses and permits at the federal, state and
municipal levels.
Bio-medical Waste (Management & Handling) Rules, 1998 have defined Bio-Medical as a type of bio-waste because of the possibility
that it might contain hold bodily fluids like blood or other contaminants prescribed thereunder. These rules were prescribed by the
Ministry of Environment & Forests (MoEF) which was formed under the Environment (Protection) Act, 1986.
Bio-medical Waste Authorisation is a mandatory authorisation issued under the provisions of Bio-medical Wastes Management Rules, 2016 to the persons responsible for the generation or collection or reception or storage or transportation or treatment or disposal or any other manner of handling of biomedical wastes listed in Schedule 1 of the Bio-medical Wastes Management Rules, 2016. Medical wastes, which is generated during the diagnosis, treatment or immunization of human beings or animals or in research activities pertaining thereto or in the production or testing of biological, and including categories mentioned in Schedule I, of the BMW rules, 2016 is called as Bio-Medical Waste. Clinics, hospitals, labs and other medical establishments which generate, collects, stores, transport, dispose of, this bio-medical waste needs to set-up the requisite mechanism for the efficient disposal of generated waste either directly or through a common biomedical waste treatment and disposal facility (ies). Untreated disposal of medical waste will cause environmental pollution, unpleasant smell, and growth and leads to develop insects, rodents and worms and may lead to the transmission of diseases like typhoid, cholera, hepatitis and AIDS through contaminated syringes and needles with an infected human. Hence, The Bio-Medical Waste Management Rules, 2016 have been notified to efficiently manage the generated bio-waste in the country. Every occupier or operating handling bio-medical waste, irrespective of quantity, is required to obtain authorization under section 10 of bio-medical waste management rule 2016.
Bio-medical Waste Authorisation is an authorisation issued under the provisions of Bio-medical Wastes Management Rules, 2016 for the generation or collection or reception or storage or transportation or treatment or disposal or any other manner of handling of biomedical wastes listed in Schedule 1 of the Bio-medical Wastes Management Rules, 2016.
Startup India is a flagship initiative of the Government of India aimed at catalyzing the community of startups
and creating a healthy and inclusive ecosystem for innovation and entrepreneurship in India. After the launch
of the initiative on 16 January 2016, Startup India has launched many initiatives aimed at empowering
entrepreneurs and turning India into a nation of job-creators instead of job-seekers.
RNI STANDS FOR THE REGISTRAR OF NEWSPAPERS OF INDIA. RNI registration is a mandatory requirement to start a business of newspapers, magazines or journals in India. In India all the publishing industry is governed under the press and books registration act, 1867. Nowadays this is one of the most rapidly growing industry. All the daily, weekly, month newspapers, magazine or journals are required to get them self-registered under Registrar of Newspaper for India, which is governed by the ministry of information and broadcasting. This Ministry is responsible for controlling and framing rule regulation for Registrar of Newspaper for India (RNI) under the press and registration of books act, 1867.
Public limited company registration proposal cvplcorpzo
It is a form of business which is came into existence through companies act. It is a form of business having separate
legal entity from its promoter just like other forms of company. The main advantage of Public limited form of
company is that it can raise capital from the public, it can transfer its share from one person to another, and there is
more opportunity of growth and expansion under this form of company and many more
The factory owners are required to notify and also register their premises with the local governing authority before the beginning of operations. This helps in facilitating the risk management at workplace and the total implementation of Safety and Health Management Systems in factory premises The Factories Act 1948 states that a factory must obtain approval from the labor and employment department for its building plan before it covers itself for registration of a factory. Under this act, Factory license registration and renewal is also done to ensure the safety of workers
DPCC दिल्ली प्रदूषण नियंत्रण समिति के लिए है जो एक ऐसा निकाय है जो यह सुनिश्चित करता है कि उद्योग / व्यवसाय दिल्ली राज्य में प्रदूषण / दहन स्तरों की विनियमित सीमाओं के भीतर काम कर रहे हैं और प्रत्येक व्यवसाय को उनकी श्रेणी के आधार पर उनकी श्रेणी के अनुसार अनापत्ति प्रमाण पत्र प्रदान करते हैं। प्रदूषक एक उद्योग / प्रतिष्ठान जारी करता है, ये एनओसी (अनापत्ति प्रमाण पत्र) दो चरणों में आते हैं जैसे कि सीटीई / सीटीओ अर्थात संस्थापित करने और सहमति देने के लिए कार्य करना।
Biomedical waste authorisation is an authorisation granted under the Bio-Medical Waste Management Regulations, 2016, to generate or collect, receive, transport, or disposal or otherwise manage biomedical wastes lists in Schedule 1 of the Regulations.
Know all about the FSSAI Registration and its significance on your businessEstartupindia.com
Food safety & hygiene has become a global concern in today’s world. If you want to grab maximum client attention in your business of food manufacturing & processing, learn about the fundamentals of food license and how it can boost the growth of your food business at the highest level.
WHAT IS FSSAI REGISTRATION, LICENCE, Proposal?corpzo
FSSAI registration is compulsory for all food businesses who are involved in a small food business. The
small food business operator can be any person or entity who fulfils below criteria based on SIZE AND
NATURE:
SITRA stands for South India Textile Research Associationcorpzo
SITRA stands for South India Textile Research Association, established in 1956 is governed by a council
administration consisting of a member representative of the industry, government, and scientists. It
sponsored by the ministry of textile of the government of India. It is governed by a council of
administration composed of twenty-five members, including representatives from reputed institutions
from industry, central and state governments, and scientists.
CDSCO and Medical Device Registration in IndiaASC Group
To obtain CDSCO registration in India, you need to make an application online by signing up on the Sugam CDSCO portal. After specifying the registration purpose and entering all the necessary details, you shall submit the registration online. Apply Now With ASC Group for CDSCO and Medical Device Registration.
As per the RBI guidelines Payment Aggregators are entities that facilitate e-commerce sites and merchants to accept various payment instruments from the customers for completion of their payment obligations without the need for merchants to create a separate payment integration system of their own. PAs facilitate merchants to connect with acquirers. In the process, they receive payments from customers, pool and transfer them on to the merchants after a time period. For achieving this, a Payment Aggregator undergoes a comprehensive process of integration with all the payment service providers and consolidates this on a single platform.
Food Safety and Standards Authority of India (FSSAI) is an autonomous body established under the Ministry of Health & Family Welfare, Government of India with the vision of maintaining food hygiene standards
The registration provides the right to sue those who try to copy your trademark. And no one else can use a
trademark identical to another person's registered one. You will use an “R” symbol for it until you file a
trademark and it will be valid for up to 10 years from the date of registration. Within 3 days you can easily
obtain a TM. But, it takes up to 2 years to get ®
Compliance is the key to sustenance of a business. Corpzo ensures hassle-free compliance for your business. We offer tailor-made services comprising of incorporation, finance, compliance, business strategy and marketing consulting, legal services, compliance and regulatory advisory. We have you covered from incorporation to growth, from compliance to sustenance and from finance to marketing functions.
Vaginal tightness use etumax honey for men or etumax for menSatyapal Singh
Keep in mind, to investigate what feels better and what positions are agreeable and effortless for the both of you. Overcome loss of libido with etumax Honey for Men or etumax for Men.
Power Monitoring Device records 34 PARAMETERS of Power in an EXCEL SHEET that further can show in more high lighted form of GRAPHS as to how their POWER USAGES are taking place in their premises.Green Dot manufactures both these devices of quality .
Shorting of more than one turn through Carbon Brush.( Voltage per turn affect). In windings with thinner wires that have high resistance perturn - this heating is lower in comparison to large heating on thicker wires. In Dimmers of 2 Amps, -this heating is very low in comparison to 200 A coil
Power point of automatic power factor controllerSatyapal Singh
Green Dot Electric Limited has developed a Variac Based Power Factor Panel. A Motorised
Variable Transformer ( the Motorised Dimmer Dot ) is used a source of Variable Voltage
that is applied to the required value of Capacitance rated for 440 Volts or so.
Wireless energy monitoring www.opto22.com documents 1936_opto_emu_sensor_data...Satyapal Singh
Similarly in Power Factor Controllers, in the 1st Stage – fixed value capacitors are added in parallel to individual motors or loads. This is a Crude method of Power Factor Correction.
If You can purchase any kind of electrical product for saving the electricity light,electricity bill and power saving,Than you can visit this website www.greendotindia.com
"𝑩𝑬𝑮𝑼𝑵 𝑾𝑰𝑻𝑯 𝑻𝑱 𝑰𝑺 𝑯𝑨𝑳𝑭 𝑫𝑶𝑵𝑬"
𝐓𝐉 𝐂𝐨𝐦𝐬 (𝐓𝐉 𝐂𝐨𝐦𝐦𝐮𝐧𝐢𝐜𝐚𝐭𝐢𝐨𝐧𝐬) is a professional event agency that includes experts in the event-organizing market in Vietnam, Korea, and ASEAN countries. We provide unlimited types of events from Music concerts, Fan meetings, and Culture festivals to Corporate events, Internal company events, Golf tournaments, MICE events, and Exhibitions.
𝐓𝐉 𝐂𝐨𝐦𝐬 provides unlimited package services including such as Event organizing, Event planning, Event production, Manpower, PR marketing, Design 2D/3D, VIP protocols, Interpreter agency, etc.
Sports events - Golf competitions/billiards competitions/company sports events: dynamic and challenging
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"𝐄𝐯𝐞𝐫𝐲 𝐞𝐯𝐞𝐧𝐭 𝐢𝐬 𝐚 𝐬𝐭𝐨𝐫𝐲, 𝐚 𝐬𝐩𝐞𝐜𝐢𝐚𝐥 𝐣𝐨𝐮𝐫𝐧𝐞𝐲. 𝐖𝐞 𝐚𝐥𝐰𝐚𝐲𝐬 𝐛𝐞𝐥𝐢𝐞𝐯𝐞 𝐭𝐡𝐚𝐭 𝐬𝐡𝐨𝐫𝐭𝐥𝐲 𝐲𝐨𝐮 𝐰𝐢𝐥𝐥 𝐛𝐞 𝐚 𝐩𝐚𝐫𝐭 𝐨𝐟 𝐨𝐮𝐫 𝐬𝐭𝐨𝐫𝐢𝐞𝐬."
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At its core, generative artificial intelligence relies on the concept of generative models, which serve as engines that churn out entirely new data resembling their training data. It is like a sculptor who has studied so many forms found in nature and then uses this knowledge to create sculptures from his imagination that have never been seen before anywhere else. If taken to cyberspace, gans work almost the same way.
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2. A
YUSH ADVISORY
+91- 99991 39391 reach@corpzo.com www.corpzo.com
www.corpzo.com
A
YURVEDA (A
yush)
MANUFACTURING LICENCE
3. ACCELERATING BUSINESS EVOLUTION
✓ We are a Corporate Compliance organization having our presence across the globe aiming to ease compliance
and assist in business evolution.
✓ We ensure that your business is up to pace with todays hyper-dynamic corporate legal structure(s)
✓ We take care of your compliance, so you can focus on your business.
✓ We are a corporate compliance organisation with expertise at providing pollution related and waste
management advisory.
✓ We have facilitated more 5000+ clients in attainment of there business licences and registrations and more than
300 clients in obtaining there Ayush Manufacturing Licences throughout India.
ABOUT US
4. WHAT IS A
YUSH LICENCE?
APPL
Y NOW
Read more
Ayurveda which literally means “The Science of Life” is one of the oldest healing science to have ever existed dating back
almost 5000 years or more. Ayurveda originated from the ancient Vedic culture and is the basis of the principles of many of
the natural healing systems now familiar in the West have their roots in Ayurveda, including Homeopathy and Polarity
Therapy.
Ayush Stands for Ayurveda, Yoga & Naturopathy, Unani, Siddha and Homoeopathy and every business engaged in the
manufacture, Retail, Wholesale or any other form of trade of Ayurvedic or Herbal Products should get an Ayush Licence
issued by the Ministry of AYUSH . The Ministry of AYUSH is responsible for development, education, research and growth
of the alternative medicine system in India.
Any manufacturer of Ayurvedic or Herbal products or medicines in India is required to obtain a license from the
Department of AYUSH which is established and regulated by the Ministry of AYUSH.
5. a
yush manufacturing licence
UNANI PRODUCTS
HERBAL HEALTH SUPPLEMENT
AYURVEDIC DRGUS / PRODUCTS
HERBAL DRUGS
HERBAL COSMETICS
For Manufacturing & Marketing of Ayush Products
Manufacturing Unit is a must
GMP Certification is mandatory
For third party or contract manufacturing
May use manufacturing unit of third party
Third party manufacturing unit should be GMP Certified
SELF
MANUFACTURING
THIRD PARTY
MANUFACTURING
6. A
YUSH PRODUCT CLASSIFICATION
Ayurvedic Medicines are generally made of organic and pure
ingredients found in nature like condiments, herbs and roots.
Ayurvedic products are known to be free of any chemicals and
dangerous ingredients.
AYURVEDIC DRUGS
01 Herbal supplements are a form of supplement that has plant or
portion of herbaceous plants used for its own flavour, odour, or
potential therapeutic properties.
HERBAL HEALTH SUPPLEMENT
02
Ayurvedic Herbal Products are also formulated using ancient
Ayurveda. These goods formulated from the composition of the
extract of herbs and various other herbal components
comprising of different types of woods turmeric and some
condiments.
HERBAL COSMETICS
03 Unani medicine is a system of alternative medicine which was
originally practiced ancient Greece but is now practiced
primarily in India. Unani system of medicine uses alternative
therapies, herbal remedies and dietary practices to prevent and
treat diseases.
UNANI DRUGS
04
The system of Medicines which uses a herb or a plant or a part
of a plant as medication or more likely as supplements are cove
red in Herbal Drugs. These medicines or drugs are mostly used t
o maintain a healthy lifestyle and increased wellbeing.
HERBAL DRUGS
05
7. Mandatory requirements
✓ UNIT LOCATION: Manufacturing unit should be situated in an industrial area.
✓
MINIMUM SIZE OF UNIT: Should have a minimum of three rooms (1 for Raw Material, 1 for Finished
products and an Office Room)Certification.
✓ GMP CERTIFICATE is Mandatory.
✓ TEAM SPECIFICATIONS: There is a professional required for the team.
✓ INSPECTION: Inspection by Drug Inspectors is one of the requisites for approval of the licence.
✓ LOAN MANUFACTURING AGREEMENT should be signed between the two parties.
8. ✓ MOA & AOA (in case of Company)
✓ Rent Agreement.
✓ Aadhar Card and PAN card of authorized signatory.
✓ PAN card of the business Entity (other than proprietorship)
✓ An affidavit confirming the compliance of MPD 2021
✓ Proof of Qualification of the respective personnel
✓ Layout Plan/Site Plan of the Premises
✓ Details of plot area and built up area
✓ Registration of the state Ayush Council/department
✓ Electricity Bill / Proof of Occupancy
✓ Certificate by a Chartered Accountant certifying total cost of
project
✓ Detailed project report
✓ Appointment Letter and detailed profile of the
director/partners of the company.
✓ Factory/Trade/Health Trade Licence
✓ Contact Information (i.e. email id, mobile number) Letter head
Requisite Documents & Information
In case any further information or document is required, Our Compliance team will collect the same within 7 days begin the process.
9. Steps for A
yush licence
SITE PLAN
FILE SUBMISSION
APPROVAL
Review of the duly signed and executed
Documents by the Department Officials
Submission of application with prescribed
fees post which the Challan is submitted.
Approval of the Site Plan / Layout Map
from the respective State Authority
The file is meticulously scrutinized
followed by a site inspection of the Unit
AYUSH LICENCE is issued on
satisfactory inspection and positive
scrutiny of the application filed by the
applicant.
Collection & Verification of Soft Copy
of all the relevant Documents &
Information.
10. SCOPE OF WORK
✓ Site Visit & Collection of Documents by our Expert ✓ Preparation of Draft Application and Attachments
✓ Submission of Application and prescribed fees
✓ Submission of Application and prescribed fees
✓ END TO END Advisory for Ayush Licence
✓ Pro-active follow up with the designated officer
11. 01
02
03
05
04
Assistance in development of
Formulations
RELATED SERVICES
Consultation for Good Manufacturing
Practice (GMP)certificate
Providing textual and research reference
for ingredients of the different disease.
Evaluation of formulation as per prescribed
drugs license format.
Consultation for development of Formulations
06
Advisory for preparation of Consumer Reports
12. Our Services
Environment Approvals
o Pollution Noc/Consent
o EPR Authorisation (E-waste & Plastic)
o Bio Medical Waste
o Solid Waste
o Hazardous Waste
o CGWA NOC
Transaction Support
o Transaction Advisory
o Due Diligence
o Mergers & Acquisition
o IPO & FPO
Intellectual Property
o Trademark
o Patent
o Copyright
o Representation & Appeal
Financial Advisory
o Accounting & Book Keeping
o Loans & Funding
o VCFO Services
o International Accounting
o Credit Rating Advisory
o Startup Funding
o Project Evaluation
Business Incorporation
o Indian Business Incorporation
o International Incorporation
o Foreign Subsidiary / India Entry
o Financial Business Incorporation
o NGO Incorporation
o Joint Ventures/Speacial Purpose Vehicles
o Trust/ Society/ Section 8/ NGO
Steps to a
Successful
Business
02
Licence & Registration
o Labour Licences
o RBI Licences
o Drug & Cosmetics
o Ayush & Herbal
o Urban Local Body Approval
o Regulatory Approvals
Compliance Management
o Annual Compliance
o Periodic Filing and Returns
o Change in Business
o FERA & FEMA
o Listing Compliance
Business Strategy
o Business Plan
o Startup Pitch Deck
o Feasibility Analysis
o Techno Economic Evaluation
01
03
04
05
06
07
08
13. OUR APPROACH Our processes are aimed at solving
most complex business problems,
reducing risk and gain a competitive
advantage by achieving good
governance and financial control
Understanding the client’s business needs and
analyzing the requirements on call or in person as
the need be
ASSESSING REQUIREMENTS
We align a professional to ensure to discuss in
detail the compliance requirements of your
business and thorough assistance throughout the
process.
DEDICATED PROFESSIONAL
We thrive to keep you apprised about the status of
your application until its completion. Every
development on your application is brought to
your attention.
REGULAR UPDATES
We share the estimated expenses and a service
level agreement for the requested service
SIGNING OF SLA
Following the SLA the necessary documents and
information are collected from the client
DOCUMENTS & INFORMATION
Stage 1 Stage 3 Stage 5
Stage 2 Stage 4
14. 2000 +
Happy Clients
Across Industry Verticals
Around the Globe
Our Presence and Growth
Significant
Growth in Client
Base Last 3 Years
FMCG
Information
Technology
Automobile
Textile
Packaging
& Printing
Metals &
Minerals
Financial
Services
Healthcare
&
Pharmaceuticals
Waste
Management
Energy &
Natural
Resources
Real
Estate
Consumer
Retail
Food &
Beverages
Banking &
Insurance
145 40 110 400 754 545 900 525
850 100 50 350 75 200 400
2013
171 Clients
2017
813 Clients
2020
2010
Clients
OUR PRESENSE ACROSS INDUSTRY VERTICALS around the globe
15. CO R P Z O
PROMISE
Why Us?
✓ W e p ro mi s e p e rf e c t i o n !
✓ W e p ro mi s e b u s i n e s s e vo l u t i o n !
✓ W e e n s u re a c c u ra c y!
✓ W e b e l i e ve i n b u s i n e s s i d e a s !
✓ W e p ro mi s e OUR B E S T!
16. Who we are
We believe in empowering businesses.
Corpzo is an initiative by Ultiwise Ventures Private Limited with a team of more than 1000 legal, finance and banking professionals, set out to
assist entrepreneurs around the globe in their business quests. We believe that every business needs nourishment in its budding stages. Ensuring
smooth navigation through the bumpy ride of legal compliance, financial risks is what we are good at.
We understand that the journey of an entrepreneur begins with his idea of a business. We, at, Corpzo, offer a complete range of professional
services and tailor-made solutions for the evolution of your business ranging from incorporation compliance, legal, financial, taxation,
technology, Intellectual Property Management, Registrations, Licensing and Marketing.
We assist you in choosing the best suited mode of business, get appropriate protection for your intellectual property, attain all the relevant
mandatory and voluntary registrations, approvals, permits and certifications. We also assist in managing the accounts, taxation, finance and
funding aspects of your business. In essence we wish for you to concentrate on your idea while we focus on the rest for you.
Our team of experts aims at easing Compliance and incubating your business growth with maximum efficiency & minimalist timeline.
ALL YOU NEED TO DO IS CALL US AND LET US WORRY ABOUT THE REST !! IT’S THAT EASY!!
Technology Based Compliance Platform