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Contract manufacturing organizations pharmaceutical

Contract manufacturing organizations pharmaceutical Specification

Indication
According to prescribed formulation and therapeutic area

Dosage Form
Solid, Liquid, Semi-solid

Origin of Medicine
Indian origin

Pacakaging (Quantity Per Box)
Customized packaging as per client requirement

Salt Composition
Customized as per client product

Drug Type
Generic and Branded formulations

Ingredients
Active pharmaceutical ingredients (APIs) as per client requirement

Physical Form
Tablets, Capsules, Syrups, Injections, Ointments

Function
Therapeutic/Medicinal

Recommended For
Pharmaceutical companies seeking contract manufacturing services

Dosage
As prescribed by healthcare professional

Dosage Guidelines
Follow directions provided by the prescribing physician

Suitable For
Adults, Children (depending on formulation)

Quantity
Customized as per order specifications

Storage Instructions
Store in a cool, dry place, away from direct sunlight

Quality Control
Stringent QC and QA processes

Contract Types Offered
Full development, technology transfer, finished dosage manufacturing

Labeling
Customizable packaging and labeling

Manufacturing Compliance
GMP, WHO-GMP certified facilities

Regulatory Support
Documentation and regulatory filing assistance available

Export Capability
Global export facility available

Batch Size
Scalable production batch sizes

Lead Time
48 weeks based on order specifications

Transportation
Temperature-controlled logistics if required

Minimum Order Quantity
As per agreement with client

Shelf Life
Typically 24-36 months based on formulation

About Contract manufacturing organizations pharmaceutical

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contract manufacturing organizations pharmaceutical in Surat

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contract manufacturing organizations pharmaceutical in India

Manufacturing Excellence & Compliance

Our manufacturing units are fully compliant with GMP and WHO-GMP standards, guaranteeing the highest level of product quality and safety. Each facility is designed for flexibility and scalability, enabling us to accommodate variable batch sizes and complex product requirements while adhering to stringent regulatory guidelines.

Customizable Solutions for Every Client

We offer a tailored approach, producing generic and branded formulations as per your specifications. From dosage form and packaging to active pharmaceutical ingredients and labeling, every aspect can be customized. Minimum order quantities and batch sizes are determined collaboratively to meet your unique business needs.

Trusted Partner for Global Exports

Our infrastructure supports worldwide distribution, featuring temperature-controlled logistics and robust quality assurance processes. We provide comprehensive documentation and regulatory filing assistance, ensuring a smooth import/export experience and reliable delivery of pharmaceutical products globally.

FAQ's of Contract manufacturing organizations pharmaceutical:

Q: How does your organization ensure manufacturing compliance?

A: We operate GMP and WHO-GMP certified facilities, implementing strict quality control (QC) and quality assurance (QA) protocols throughout the manufacturing process to ensure every product meets international safety and quality standards.

Q: What types of products and dosage forms can you manufacture?

A: We can manufacture a wide range of pharmaceutical products, including tablets, capsules, syrups, injections, and ointments, across solid, liquid, and semi-solid dosage forms as specified by the client.

Q: When can I expect my order to be fulfilled?

A: Lead times typically range from 4 to 8 weeks, depending on order specifications, batch size, and customization requirements. Final timelines are agreed upon during contract finalization.

Q: Where are your manufacturing facilities located and do you export globally?

A: Our GMP and WHO-GMP certified facilities are located in India, and we are well-equipped for global export, providing temperature-controlled logistics as needed to ensure product integrity during transit.

Q: What is the process for initiating a contract manufacturing agreement?

A: The process begins with a consultation to determine your requirements, followed by agreement on batch size, minimum order quantity, formulation specifications, and contract type (full development, technology transfer, or finished dosage manufacturing). We then manage regulatory documentation and production as per the agreed timeline.

Q: How can your services benefit my pharmaceutical company?

A: Partnering with us enables access to scalable production, regulatory support, custom solutions, and global export capabilities. This helps reduce operational overhead, ensures compliance, and optimizes supply chain efficiency.

Q: What are the storage and usage guidelines for the products?

A: Products should be stored in a cool, dry place, away from direct sunlight. Dosage and usage should always follow directions provided by a healthcare professional, and are customized as per formulation and therapeutic area.