Service Mode	Offline
Service Duration	24 Months
Certification	WHO, ISO, GMP, GLP
Pharmaceutical Experience	Above 10 Years
Delivery Time	Within a Month
Type of Injection	Lyophilized, Subcutaneous, Intravenous, Intramuscular
Form of Medicine	Protein Powder, Tablet, Ointments, Injection, Syrup, Capsule
Production Capacity	Medium Scale, Large Scale, Small Scale
Number Of Existing Clients	100
Promotional Material	Visiting Cards, Calendars, Notepads, Diaries, Bottle, Visual Aids, Writing Pads, Pens, Working Bag, Brochure
Range of Products	Gynaecology, Antimicrobials, Antibiotics, Antihistamines, Antacids, Orthopedic, Neurological, Pediatrics, Ophthalmic, Cardiac Diabetic, Derma
Product List Available	Yes
Medicine Type	Allopathic
Payment Mode	Online
Service Location	Pan India

Pharmaceutical third-party manufacturing, also known as contract manufacturing or private label manufacturing, is a business arrangement where a pharmaceutical company (the third party) outsources the manufacturing of its products to another company, typically a specialized contract manufacturing organization (CMO). This is a common practice in the pharmaceutical industry and offers several advantages.

 

Here's an overview of how pharmaceutical third-party manufacturing services typically work:

 

Outsourcing Agreement: The pharmaceutical company seeking manufacturing services enters into an outsourcing agreement with a third-party manufacturer (CMO).

 

Product Formulation and Development: The pharmaceutical company provides the CMO with the formula, specifications, and other necessary details related to the drug or product to be manufactured.

 

Regulatory Compliance: The CMO is responsible for ensuring that the manufacturing processes comply with regulatory standards and requirements set by health authorities. This includes Good Manufacturing Practice (GMP) standards.

 

Production: The CMO carries out the production of the pharmaceutical products based on the specifications provided. This may include manufacturing tablets, capsules, injections, or other dosage forms.

 

Quality Control: The CMO conducts quality control and testing to ensure that the products meet the required quality standards. This is a crucial step to ensure the safety and efficacy of the pharmaceuticals.

 

Packaging and Labeling: The CMO is often responsible for packaging and labeling the products according to the specifications provided by the pharmaceutical company. This may include custom packaging with the pharmaceutical company's branding.

 

Distribution: Once the products are manufactured, tested, packaged, and labeled, they are typically shipped back to the pharmaceutical company or directly to distributors for further distribution.

 

Benefits of Pharmaceutical Third-Party Manufacturing:

 

Cost Efficiency: The pharmaceutical company can focus on research, marketing, and sales without the need for extensive in-house manufacturing facilities.

 

Flexibility: The company can scale production up or down based on demand without the burden of maintaining a fixed production capacity.

 

Expertise: CMOs often have specialized knowledge and experience in manufacturing, ensuring high-quality production.

 

Regulatory Compliance: CMOs are expected to adhere to strict regulatory standards, reducing the regulatory burden on the pharmaceutical company.

 

It's important for pharmaceutical companies to carefully choose a reliable and reputable third-party manufacturer to ensure the quality and compliance of their products. Additionally, clear communication and a well-defined contractual agreement are crucial for the success of the partnership.

Additional Information:

• Item Code: INJ09
• Production Capacity: 500000
• Delivery Time: 40 to 60 Days
• Packaging Details: As per requirements.

Certification	GLP, WHO, GMP
Pharmaceutical Experience	Above 5 Years
Delivery Time	Within a Month
Form of Medicine	Tablet, Capsule, Syrup
Type of Injection	Subcutaneous, Intravenous, Lyophilized, Intramuscular
Production Capacity	Medium Scale, Large Scale
Number Of Existing Clients	100
Product Available	Injection Tablet Capsule

Pharmaceutical third-party manufacturing, also known as contract manufacturing or private label manufacturing, is a business arrangement where a pharmaceutical company (the third party) outsources the manufacturing of its products to another company, typically a specialized contract manufacturing organization (CMO). This is a common practice in the pharmaceutical industry and offers several advantages.

 

Here's an overview of how pharmaceutical third-party manufacturing services typically work:

 

Outsourcing Agreement: The pharmaceutical company seeking manufacturing services enters into an outsourcing agreement with a third-party manufacturer (CMO).

 

Product Formulation and Development: The pharmaceutical company provides the CMO with the formula, specifications, and other necessary details related to the drug or product to be manufactured.

 

Regulatory Compliance: The CMO is responsible for ensuring that the manufacturing processes comply with regulatory standards and requirements set by health authorities. This includes Good Manufacturing Practice (GMP) standards.

 

Production: The CMO carries out the production of the pharmaceutical products based on the specifications provided. This may include manufacturing tablets, capsules, injections, or other dosage forms.

 

Quality Control: The CMO conducts quality control and testing to ensure that the products meet the required quality standards. This is a crucial step to ensure the safety and efficacy of the pharmaceuticals.

 

Packaging and Labeling: The CMO is often responsible for packaging and labeling the products according to the specifications provided by the pharmaceutical company. This may include custom packaging with the pharmaceutical company's branding.

 

Distribution: Once the products are manufactured, tested, packaged, and labeled, they are typically shipped back to the pharmaceutical company or directly to distributors for further distribution.

 

Benefits of Pharmaceutical Third-Party Manufacturing:

 

Cost Efficiency: The pharmaceutical company can focus on research, marketing, and sales without the need for extensive in-house manufacturing facilities.

 

Flexibility: The company can scale production up or down based on demand without the burden of maintaining a fixed production capacity.

 

Expertise: CMOs often have specialized knowledge and experience in manufacturing, ensuring high-quality production.

 

Regulatory Compliance: CMOs are expected to adhere to strict regulatory standards, reducing the regulatory burden on the pharmaceutical company.

 

It's important for pharmaceutical companies to carefully choose a reliable and reputable third-party manufacturer to ensure the quality and compliance of their products. Additionally, clear communication and a well-defined contractual agreement are crucial for the success of the partnership.

Additional Information:

• Item Code: 10101
• Production Capacity: 500000
• Delivery Time: 45 Days
• Packaging Details: As Per Requirements

Certification	WHO
Pharmaceutical Experience	Above 5 Years
Delivery Time	Within a Month
Form of Medicine	Tablet, Syrup, Capsule
Production Capacity	Small Scale, Medium Scale, Large Scale
Number Of Existing Clients	100+
Services	Third Party Contract Manufacturing
Dosage Form	Injection Tablet Capsule etc

Wizard Venture

(A Complete Pharma Solution)

 

Welcome to Wizard Venture Pharmaceuticals, a pioneering pharmaceutical company committed to reshaping the landscape of healthcare through innovation, excellence, and a steadfast dedication to improving lives. Established in 2022, Wizard Venture Pharmaceuticals has rapidly ascended to the forefront of the pharmaceutical industry, driven by a relentless pursuit of scientific advancement and a deep-rooted commitment to addressing unmet medical needs.

 

At the heart of our mission is a simple yet profound aspiration: to create a healthier world. We believe that every individual deserves access to high-quality and transformative healthcare solutions, and we are resolute in our mission to make this vision a reality.

 

Our Core Values:

 

Innovation: We are catalysts of change, embracing a culture that values and encourages the spirit of innovation. Our commitment to pushing the boundaries of scientific discovery fuels our quest to bring novel and effective treatments to patients around the globe.

 

Integrity: At Wizard Venture Pharmaceuticals, integrity is non-negotiable. We conduct our business with the utmost ethical standards, ensuring transparency, honesty, and accountability in all our endeavors.

 

Collaboration: We recognize that the path to groundbreaking solutions is paved through collaboration. We actively seek partnerships with healthcare professionals, research institutions, and organizations to leverage collective expertise and drive meaningful advancements in healthcare.

 

Patient-Centricity: Every decision we make is guided by a profound commitment to the well-being of patients. We understand that behind every medication is a life waiting to be improved, and we strive to develop therapies that make a tangible difference in the lives of individuals and their families.

 

 

Our Services:

We are leading supplier of best quality Pharmaceutical Products which are manufactured under CGMP-WHO norms. We are committed to serve you the best possible way by providing following services.

1.      Third Party manufacturing of various dosage form of Pharmaceutical Products covering the range. (FOR HUMAN WELNESS)

a)      Pharmaceutical Injection.

b)     Tablet.

c)      Capsule.

d)     Ointment.

e)      Syrups.

f)       Ayurvedic Products.

g)      Softgel Capsules

h)     Hard Gelatin Capsule 

2.      PCD Franchise of above mentioned formulation with fully Mono Poly Rights.

3.      Veterinary Products such as Injection, Bolus, Liquid Oral in Third Party / Contract manufacturing and in PCD Franchise with Mono Poly Right.

 

Additional Information:

• Item Code: 2025BB
• Production Capacity: 500000
• Delivery Time: Immediate
• Packaging Details: As per Requirements

Service Mode	Offline
Service Duration	3 Days
Duration	24 Months
Distribution Preferred	Single Party Distribution
Certification	WHO, GMP, GLP, ISO
Form of Medicine	Tablet, Protein Powder, Capsule, Syrup, Injection
Medicine Type	Allopathic
Promotional Material	Calendars, Pens, Visual Aids, Writing Pads, Brochure, Working Bag
Range of Products	Ophthalmic, Pediatrics, Neurological, Antimicrobials, Antibiotics, Gynaecology, Derma
Location	Pan India
Pharmaceutical Experience	Yes

Pharmaceutical third-party manufacturing, also known as contract manufacturing or private label manufacturing, is a business arrangement where a pharmaceutical company (the third party) outsources the manufacturing of its products to another company, typically a specialized contract manufacturing organization (CMO). This is a common practice in the pharmaceutical industry and offers several advantages.

 

Here's an overview of how pharmaceutical third-party manufacturing services typically work:

 

Outsourcing Agreement: The pharmaceutical company seeking manufacturing services enters into an outsourcing agreement with a third-party manufacturer (CMO).

 

Product Formulation and Development: The pharmaceutical company provides the CMO with the formula, specifications, and other necessary details related to the drug or product to be manufactured.

 

Regulatory Compliance: The CMO is responsible for ensuring that the manufacturing processes comply with regulatory standards and requirements set by health authorities. This includes Good Manufacturing Practice (GMP) standards.

 

Production: The CMO carries out the production of the pharmaceutical products based on the specifications provided. This may include manufacturing tablets, capsules, injections, or other dosage forms.

 

Quality Control: The CMO conducts quality control and testing to ensure that the products meet the required quality standards. This is a crucial step to ensure the safety and efficacy of the pharmaceuticals.

 

Packaging and Labeling: The CMO is often responsible for packaging and labeling the products according to the specifications provided by the pharmaceutical company. This may include custom packaging with the pharmaceutical company's branding.

 

Distribution: Once the products are manufactured, tested, packaged, and labeled, they are typically shipped back to the pharmaceutical company or directly to distributors for further distribution.

 

Benefits of Pharmaceutical Third-Party Manufacturing:

 

Cost Efficiency: The pharmaceutical company can focus on research, marketing, and sales without the need for extensive in-house manufacturing facilities.

 

Flexibility: The company can scale production up or down based on demand without the burden of maintaining a fixed production capacity.

 

Expertise: CMOs often have specialized knowledge and experience in manufacturing, ensuring high-quality production.

 

Regulatory Compliance: CMOs are expected to adhere to strict regulatory standards, reducing the regulatory burden on the pharmaceutical company.

 

It's important for pharmaceutical companies to carefully choose a reliable and reputable third-party manufacturer to ensure the quality and compliance of their products. Additionally, clear communication and a well-defined contractual agreement are crucial for the success of the partnership.

Additional Information:

• Item Code: P01
• Production Capacity: 50000
• Delivery Time: 40 to 60 days after approval of Art Work
• Packaging Details: As per requirements

Strength	500 mg
Injection Site	IV & IM
Prescription/Non prescription	Prescription
Form	Powder
Packaging Type	Vial
Shelf Life	24 Months
Composition	Acyclovir Injection 500 mg
Also gives	Third Party Manufacturing, PCD Pharma
Country of Origin	Made in India

Acyclovir is an antiviral medication commonly used for the treatment of infections caused by the herpes simplex virus (HSV) and the varicella-zoster virus (VZV). It is available in various forms, including oral tablets, topical creams, and intravenous (IV) injections.

 

Acyclovir injection is typically administered in a healthcare setting, such as a hospital, clinic, or infusion center, under the supervision of healthcare professionals. The IV form of acyclovir is often used for severe cases of HSV or VZV infections, particularly in immunocompromised individuals or those with severe complications.

 

Here are some key points about acyclovir injection:

 

Indications: Acyclovir injection is commonly used for the treatment of severe cases of herpes simplex infections, such as encephalitis (inflammation of the brain) caused by HSV, and for severe cases of varicella-zoster infections, including herpes zoster (shingles) in immunocompromised patients.

 

Administration: Acyclovir injection is administered by healthcare professionals through an intravenous (IV) line. The dosage and duration of treatment depend on the specific condition being treated, the severity of the infection, and the patient's overall health.

 

Monitoring: Patients receiving acyclovir injection are typically monitored closely for any adverse reactions or side effects. Common side effects may include nausea, vomiting, diarrhea, and headache. In rare cases, more serious side effects, such as kidney problems, may occur.

 

Precautions: It is important to inform healthcare providers about any pre-existing medical conditions, allergies, or medications the patient is taking before starting acyclovir treatment. This includes providing information about kidney function, as acyclovir is primarily excreted through the kidneys.

 

Pregnancy and Lactation: Pregnant or breastfeeding individuals should discuss the potential risks and benefits of acyclovir treatment with their healthcare providers. Acyclovir does pass into breast milk, and caution is advised.

 

Resistance: Prolonged or inappropriate use of acyclovir can contribute to the development of drug-resistant strains of the herpes virus. Therefore, it is essential to use acyclovir under the guidance of a healthcare professional and according to prescribed instructions.

 

It's important to note that the information provided here is for general informational purposes. If acyclovir injection is recommended, it should be administered by healthcare professionals, and the specific dosage and treatment plan should be determined by a qualified healthcare provider based on the individual patient's condition.

Additional Information:

• Item Code: CP023
• Production Capacity: 500000
• Delivery Time: Immediate in PCD Franchise & 40 to 60 Days in Third Party Manufacturing
• Packaging Details: 10 ml with Sterile water for Injection IP

Certification	WHO, GMP, FSSAI, ISO, GLP
Pharmaceutical Experience	Above 10 Years
Delivery Time	Within a Month
Form of Medicine	Injection, Tablet, Drops, Syrup, Infusion, Capsule, Sachets, Protein Powder, Ointments
Range of Products	Antacids, Pediatrics, Orthopedic, Derma, Gastrointestinal, Antihistamines, Ophthalmic, Cardiac Diabetic, Antibiotics, Neurological, Gynaecology, Antimicrobials
Production Capacity	Large Scale, Small Scale, Medium Scale
Number Of Existing Clients	100+
SERVICE	TABLET CAPSULE INJECTION VETERINARY PRODUCTS

Pharmaceutical third-party manufacturing, also known as contract manufacturing or private label manufacturing, is a business arrangement where a pharmaceutical company (the third party) outsources the manufacturing of its products to another company, typically a specialized contract manufacturing organization (CMO). This is a common practice in the pharmaceutical industry and offers several advantages.

 

Here's an overview of how pharmaceutical third-party manufacturing services typically work:

 

Outsourcing Agreement: The pharmaceutical company seeking manufacturing services enters into an outsourcing agreement with a third-party manufacturer (CMO).

 

Product Formulation and Development: The pharmaceutical company provides the CMO with the formula, specifications, and other necessary details related to the drug or product to be manufactured.

 

Regulatory Compliance: The CMO is responsible for ensuring that the manufacturing processes comply with regulatory standards and requirements set by health authorities. This includes Good Manufacturing Practice (GMP) standards.

 

Production: The CMO carries out the production of the pharmaceutical products based on the specifications provided. This may include manufacturing tablets, capsules, injections, or other dosage forms.

 

Quality Control: The CMO conducts quality control and testing to ensure that the products meet the required quality standards. This is a crucial step to ensure the safety and efficacy of the pharmaceuticals.

 

Packaging and Labeling: The CMO is often responsible for packaging and labeling the products according to the specifications provided by the pharmaceutical company. This may include custom packaging with the pharmaceutical company's branding.

 

Distribution: Once the products are manufactured, tested, packaged, and labeled, they are typically shipped back to the pharmaceutical company or directly to distributors for further distribution.

 

Benefits of Pharmaceutical Third-Party Manufacturing:

 

Cost Efficiency: The pharmaceutical company can focus on research, marketing, and sales without the need for extensive in-house manufacturing facilities.

 

Flexibility: The company can scale production up or down based on demand without the burden of maintaining a fixed production capacity.

 

Expertise: CMOs often have specialized knowledge and experience in manufacturing, ensuring high-quality production.

 

Regulatory Compliance: CMOs are expected to adhere to strict regulatory standards, reducing the regulatory burden on the pharmaceutical company.

 

It's important for pharmaceutical companies to carefully choose a reliable and reputable third-party manufacturer to ensure the quality and compliance of their products. Additionally, clear communication and a well-defined contractual agreement are crucial for the success of the partnership.

Additional Information:

• Item Code: 2025MN
• Production Capacity: 5000000
• Delivery Time: 30 DAYS
• Packaging Details: AS PER REQUIREMENTS

Distribution Preferred	Single Party
Certification	ISO, GMP, WHO
Pharmaceutical Experience	Above 10 Years
Delivery Time	Within 15 Days
Medicine Type	Allopathic
Promotional Material	Brochure, Visiting Cards, Visual Aids

In the pharmaceutical industry, PCD stands for Propaganda Cum Distribution, and a PCD franchise model is a business arrangement where a pharmaceutical company grants rights to individuals or entities (franchise partners) to market and distribute its products in a specific geographical area. This model is commonly used in both human and veterinary pharmaceuticals.

 

If you are interested in starting a veterinary injection business through a PCD franchise, here are the key steps and considerations:

 

Research and Choose a Reputable Pharmaceutical Company:

 

Look for pharmaceutical companies that specialize in veterinary products and have a good reputation for quality and compliance with regulatory standards.

Consider the range of veterinary injections they offer and whether it aligns with the needs of the market in your target area.

Contact the Pharmaceutical Company:

 

Reach out to the selected pharmaceutical company expressing your interest in obtaining a PCD franchise for their veterinary injection products.

Inquire about the terms and conditions, product availability, pricing, and any other relevant details.

Due Diligence and Agreement:

 

Conduct due diligence on the selected pharmaceutical company to ensure they meet regulatory standards and have a good track record.

Review the franchise agreement carefully, including terms related to distribution rights, pricing, payment terms, and support provided by the company.

Regulatory Compliance:

 

Ensure that the pharmaceutical company and its products comply with veterinary regulatory requirements in your target market.

Understand the documentation and approvals required for selling veterinary injections, and work closely with the company to obtain necessary licenses.

Market Assessment:

 

Evaluate the demand for veterinary injections in your chosen geographical area.

Identify potential clients such as veterinary clinics, hospitals, and distributors.

Establish Distribution Network:

 

Set up a distribution network to effectively reach veterinary professionals and retailers in your area.

Develop marketing strategies to promote the veterinary injection products.

Training and Support:

 

Ensure that the pharmaceutical company provides adequate training and support to help you understand their products, promote them effectively, and address any customer queries.

Quality Assurance:

 

Implement measures to maintain the quality and integrity of the veterinary injection products during storage and distribution.

Compliance and Reporting:

 

Adhere to all regulatory requirements for the storage, distribution, and promotion of veterinary injections.

Keep accurate records and report sales and other relevant data to the pharmaceutical company as required.

Starting a veterinary injection business through a PCD franchise involves a partnership with the pharmaceutical company, so it's crucial to choose a reliable partner with a strong product portfolio and a commitment to quality and compliance.

Additional Information:

• Item Code: PD
• Production Capacity: 50000
• Delivery Time: immediate
• Packaging Details: As Per Standard.