Salvat - CDMO/CMO

Discover Salvat

Salvat is a global pharmaceutical company, specialized in the production of pharmaceuticals and provision of services as a contract development and manufacturing organization (CDMO). With a specialized focus on sterile liquids in single-dose vials, we are headquartered in Barcelona, Spain, and have a subsidiary in Miami, US.

Our reach extends to over 60 countries worldwide, where we develop, manufacture, and market a diverse range of pharmaceutical products across several therapeutic areas, including ophthalmology, otolaryngology, gastroenterology, and wound care. Through strategic global alliances, we continuously innovate and contribute to enhancing patient care.

 

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Address: C./ Gall, 30-36, 08034, Esplugues de Llobregat
Spain
Spain Local time:

BFS expertise with FDA Approval for Sterile Manufacturing

USA and European Quality

Innovative solutions for ophthalmology and otorhinolaryngology

Our services:

CMO/CDMO

Production scale:

small
medium
large

Response time:

Service categories

Finished formulation / FDF

Tablets
Capsules
Topical formulation
Nasal Products
Ophthalmic products
Powders and Granules
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Employees:
500+
Established in:
1955

Upcoming events

DCAT Week

DCAT Week

In-person event

17-03-2025

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Pharma Contract Manufacturing

Pharma Contract Manufacturing

In-person event

26-03-2025

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CPHI North America

CPHI North America

In-person event

20-05-2025

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ESCRS

ESCRS

In-person event

12-09-2025

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AAO-HNS

AAO-HNS

In-person event

11-10-2025

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CPHI World Wide

CPHI World Wide

In-person event

28-10-2025

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Our services


Finished formulation / FDF

Tablets
Tablets remain a cornerstone of oral drug delivery, known for their stability and ease of administration. Manufacturing tablets involves granulation, compression, and coating techniques, ensuring consistent drug release and patient compliance. They cater to a wide range of therapeutic needs, from pain management to chronic diseases.
Contact supplier

Replies quickly

Capsules
Capsules offer a versatile solution for oral drug delivery, particularly for drugs with taste or stability issues. Their production combines gelatin or vegetarian shells with active pharmaceutical ingredients (APIs), providing targeted release profiles. Capsules are essential in both over-the-counter and prescription medicine.
Contact supplier

Replies quickly

Topical formulation
Topical formulations, including ointments and creams, are pivotal in dermatological treatments. Their production focuses on achieving the right consistency, absorption rate, and drug concentration for effective skin application, addressing conditions from eczema to infections.
Contact supplier

Replies quickly

Nasal Products
Nasal products, encompassing sprays, drops, and gels, provide targeted therapy for respiratory conditions. Their production involves creating formulations that ensure optimal viscosity and absorption through nasal mucosa, addressing allergies, congestion, and other nasal ailments.
Contact supplier

Replies quickly

Ophthalmic products
Ophthalmic products, including eye drops, are specialized for ocular conditions. Their sterile manufacturing process ensures safety and precision in treating infections, allergies, and glaucoma. The production focuses on isotonicity, pH balance, and non-irritating formulas.
Contact supplier

Replies quickly

Powders and Granules
Powders and granules are versatile in pharmaceutical manufacturing, used for oral, topical, and reconstituted products. Their production involves careful particle size control and blending for uniformity, catering to a wide range of medical applications and dosage forms.
Contact supplier

Replies quickly

Contact Salvat for Contract Services Expertise

Connect with Salvat, a leading pharmaceutical company from Spain. They offer specialized CMO/CDMO - Contract (Development) Manufacturing Organizations, of which the services for CMO/CDMO include Tablets, Capsules, Topical formulation. Contact Salvat for free and discover if they are the perfect partner for your pharmaceutical needs.

CMO/CDMO - Contract (Development) Manufacturing Organizations

CDMOs and CMOs are pivotal in the pharmaceutical and biotech industries, offering specialized services in drug development and manufacturing. They assist in scaling up production from laboratory to commercial quantities, while adhering to strict regulatory standards. These organizations play a crucial role in the efficient and cost-effective production of medical and pharmaceutical products, ensuring quality and compliance at every stage.


Pharmaoffer's category for Contract Manufacturing Organizations (CMOs) and Contract Development and Manufacturing Organizations (CDMOs) encompasses a wide range of specialized services crucial to the pharmaceutical and biotech sectors. These organizations, often referred to as pharmaceutical CDMOs or drug CMOs, are instrumental in advancing drug development and manufacturing processes.


Key Functions of CMOs/CDMOs:


  • Drug Development and Manufacturing Expertise: Offering comprehensive services in drug development, from initial research and development to full-scale manufacturing. This includes CDMO services and CMO manufacturing, ensuring a seamless transition from concept to market.

  • Scalability Solutions: Assisting in scaling production from laboratory to commercial scale, meeting the demands of various projects while maintaining quality and efficiency. This is where the expertise of a full-service CDMO becomes invaluable.

  • Regulatory Compliance and Quality Assurance: Ensuring adherence to strict regulatory standards such as FDA and EMA guidelines, and implementing rigorous quality control measures throughout the manufacturing process. This includes operating within GMP certified facilities to guarantee the highest standards of production.

  • Cost-Effective Production: Providing efficient and cost-effective solutions for the production of medical and pharmaceutical products, enabling companies to focus on innovation and marketing. CMO contract manufacturing plays a key role in this aspect.

  • End-to-End Service Provision: From concept to commercialization, CMOs/CDMOs offer a range of services including process optimization, formulation development, clinical trial material production, and commercial manufacturing. This comprehensive approach is often referred to as Contract Development Manufacturing.


Connect with Leading CMOs/CDMOs

Through Pharmaoffer, you can explore and connect with a comprehensive range of CMOs/CDMOs. Our platform offers access to organizations that play a vital role in the efficient, quality-assured, and compliant production of pharmaceutical and medical products, supporting the industry's growth and innovation. Whether you're looking for a CDMO partner, CDMO solutions, or contract manufacturers in pharma, Pharmaoffer is your gateway to the best in the industry.

Finished formulation / FDF

Finished Formulation CMOs/CDMOs focus on the final stage of pharmaceutical product manufacturing, which involves blending and formulating active pharmaceutical ingredients (APIs) into finished dosage forms like tablets, capsules, liquid formulations, and injectables.


Pharmaoffer showcases a range of Contract Manufacturing Organizations (CMOs) and Contract Development and Manufacturing Organizations (CDMOs) that specialize in Finished Formulation. These organizations, key players in FDF (Finished Dosage Formulations) manufacturing, are essential in the pharmaceutical industry, focusing on the final stage of product manufacturing – blending and formulating APIs into finished dosage forms.


Key Services Provided by Finished Formulation CMOs/CDMOs:


  • Diverse Dosage Form Production: Expertise in creating a wide array of finished dosage forms, including tablets, capsules, oral liquids, powders, and more. This service is a critical aspect of FDF CDMO offerings.

  • High-Quality Formulation Development: Developing formulations that ensure efficacy, stability, and patient acceptability, adhering to precise pharmaceutical standards. This includes specialized formulation services and CDMO formulation development.

  • Advanced Manufacturing Processes: Utilizing state-of-the-art manufacturing processes and equipment to produce high-quality finished pharmaceutical products. This is a key component of CDMO products and contract formulation services.

  • Regulatory Compliance and Quality Assurance: Ensuring all products meet stringent regulatory standards, including compliance with FDA, EMA, and other regulatory bodies’ guidelines.

  • Customized Manufacturing Solutions: Offering tailored solutions to meet the unique needs of different pharmaceutical products, from small-scale batches to large-scale commercial production. This flexibility is essential in the realm of FDF manufacturing.


Connect with Expert Finished Formulation Providers

Through Pharmaoffer, you can explore and connect with CMOs/CDMOs that specialize in Finished Formulation services. Our platform provides access to organizations equipped with the expertise and technology necessary for the efficient and compliant production of finished pharmaceutical products.

Tablets

Tablets remain a cornerstone of oral drug delivery, known for their stability and ease of administration. Manufacturing tablets involves granulation, compression, and coating techniques, ensuring consistent drug release and patient compliance. They cater to a wide range of therapeutic needs, from pain management to chronic diseases.


Pharmaoffer lists Contract Development and Manufacturing Organizations (CDMOs) that excel in the production of tablets. As a mainstay in oral drug delivery, tablets are favored for their stability, ease of administration, and versatility in catering to various therapeutic needs. This includes specialized services in Tablets Manufacturing, tablet production, and GMP tablet manufacturing.


Key Services Provided by Our Listed CDMOs:


  • Granulation and Compression: Expertise in granulation processes to prepare powder for compression, and precision in tablet compression to ensure uniformity and dosage accuracy. This is a critical aspect of solid dose manufacturing.

  • Advanced Coating Techniques: Application of various coating techniques to enhance tablet stability, modify drug release, and improve patient acceptability. This is essential in tablet formulation.

  • Consistent Drug Release Profiles: Development of tablets with controlled release profiles, ensuring consistent therapeutic effects and patient compliance.

  • Custom Tablet Formulations: Capability to create customized tablet formulations, addressing a wide range of therapeutic areas from pain management to chronic disease treatment. This is a key service offered by tablet manufacturing companies.

  • Quality Assurance and Regulatory Compliance: Strict adherence to quality standards and regulatory guidelines, ensuring the safety and efficacy of tablet products. This includes adherence to GMP standards in tablet CDMO services.


Your Go-To Source for Tablet Production

Pharmaoffer connects you with CDMOs renowned for their tablet manufacturing capabilities. Whether for generic or specialized medications, our platform ensures access to providers equipped with the latest technology and expertise for high-quality tablet production.

Capsules

Capsules offer a versatile solution for oral drug delivery, particularly for drugs with taste or stability issues. Their production combines gelatin or vegetarian shells with active pharmaceutical ingredients (APIs), providing targeted release profiles. Capsules are essential in both over-the-counter and prescription medicine.


Pharmaoffer's selection of Contract Development and Manufacturing Organizations (CDMOs) includes experts in the production of capsules, a key component of oral drug delivery systems. Capsules are particularly valuable for drugs requiring taste masking or specific stability conditions. This includes specialized services in Capsule Manufacturing, capsule filling, and pharma capsule manufacturing.


Key Services Provided by Our Listed CDMOs:


  • Custom Capsule Formulation: Development of tailored capsule formulations, combining gelatin or vegetarian shells with APIs for specific release characteristics. This is a critical aspect of capsules formulation.

  • Taste Masking and Stability: Expertise in creating capsule formulations that address taste or stability issues, enhancing patient compliance and drug efficacy.

  • Targeted Release Profiles: Advanced technologies for creating capsules with precise release profiles, including immediate, delayed, or sustained release. This is essential in capsule contract manufacturing.

  • Compliance with Regulatory Standards: Adherence to global pharmaceutical manufacturing standards, ensuring high-quality and safe capsule products. This is a key service offered by Capsule Suppliers.

  • Versatile Production Capabilities: Capacity to produce a wide range of capsule types, catering to both over-the-counter and prescription medication markets. This includes expertise in capsules CDMO services.


Find Your Capsule Production Partner

On Pharmaoffer, you can connect with CDMOs that specialize in the innovative and efficient production of capsule formulations. Whether you're focusing on generic or novel drug development, our listed CDMOs offer the expertise and technology needed for high-quality capsule manufacturing.

Topical formulation

Topical formulations, including ointments and creams, are pivotal in dermatological treatments. Their production focuses on achieving the right consistency, absorption rate, and drug concentration for effective skin application, addressing conditions from eczema to infections.


Pharmaoffer features Contract Development and Manufacturing Organizations (CDMOs) with expertise in creating topical formulations, including ointments, creams, and gels. These products play a crucial role in dermatological treatments, offering targeted relief and treatment for various skin conditions. This includes specialized services in Topical Formulation, Topical Drug Manufacturing, and Topical Medication Manufacturing.


Key Services Provided by Our Listed CDMOs:


  • Optimized Consistency and Absorption: Development of formulations with the appropriate consistency and absorption rate, ensuring effective application and skin penetration. This is a critical aspect of Topical Drug production.

  • Precise Drug Concentration: Careful formulation to achieve the right drug concentration for maximum therapeutic effect while minimizing potential side effects. This is essential in Topical Drug development.

  • Diverse Dermatological Applications: Capability to produce a range of topical formulations for treating conditions such as eczema, psoriasis, infections, and more. This versatility is key for a topical CDMO.

  • Quality Control and Stability Testing: Rigorous quality assurance processes and stability testing to ensure the safety, efficacy, and longevity of topical products. This is a fundamental service of Topical Drug CDMO.

  • Patient-Centric Formulations: Focus on patient comfort and ease of use, enhancing patient compliance and treatment outcomes.


Find Your Topical Formulation Development Partner

Through Pharmaoffer, you can connect with CDMOs specializing in the development and manufacturing of topical formulations. Our platform provides access to experts who can deliver high-quality, effective topical treatments for a wide array of dermatological needs.

Nasal Products

Nasal products, encompassing sprays, drops, and gels, provide targeted therapy for respiratory conditions. Their production involves creating formulations that ensure optimal viscosity and absorption through nasal mucosa, addressing allergies, congestion, and other nasal ailments.


Pharmaoffer connects you with Contract Development and Manufacturing Organizations (CDMOs) that specialize in the production of nasal products. These products, which include nasal sprays, drops, and gels, are designed to provide targeted therapy for various respiratory conditions. This includes expertise in Nasal Drug Delivery Systems and Nasal Drug Manufacturing.


Key Services Provided by Our Listed CDMOs:


  • Formulation Expertise: Development of nasal product formulations with optimal viscosity and absorption properties for effective delivery through the nasal mucosa. This is a key aspect of Nasal Drug Manufacturing.

  • Quality and Safety Assurance: Rigorous quality control processes to ensure the safety and efficacy of nasal products, suitable for treating allergies, congestion, and other nasal conditions. This is essential for a nasal CDMO.

  • Customized Development Solutions: Tailoring of nasal product formulations to meet specific therapeutic needs and patient preferences.

  • Regulatory Compliance: Adherence to pharmaceutical manufacturing standards and regulations, ensuring high-quality nasal product production.

  • Innovative Delivery Systems: Expertise in creating advanced nasal delivery systems that enhance the therapeutic effectiveness and patient experience.


Find Your Nasal Product Development Partner

Through Pharmaoffer, pharmaceutical professionals can easily find and collaborate with CDMOs experienced in nasal product development and manufacturing. Whether for over-the-counter solutions or prescription medications, our platform links you to providers equipped with the necessary expertise for high-quality nasal product production.

Ophthalmic products

Ophthalmic products, including eye drops, are specialized for ocular conditions. Their sterile manufacturing process ensures safety and precision in treating infections, allergies, and glaucoma. The production focuses on isotonicity, pH balance, and non-irritating formulas.


Pharmaoffer provides access to Contract Development and Manufacturing Organizations (CDMOs) with specialized expertise in ophthalmic products. These products, crucial for treating various ocular conditions, require a high level of precision and safety in their manufacturing processes, including Ophthalmic Product Manufacturing and Ophthalmic Product Solutions.


Key Services Provided by Our Listed CDMOs:


  • Sterile Manufacturing Processes: Ensuring sterile conditions in the production of ophthalmic products to maintain safety and effectiveness, especially critical for eye drops. This is a key service of an Ophthalmic CDMO.

  • Isotonicity and pH Balance: Focus on formulating ophthalmic products with appropriate isotonicity and pH balance to ensure comfort and efficacy in ocular treatments.

  • Non-Irritating Formulas: Development of gentle, non-irritating formulas suitable for sensitive eye tissues, addressing conditions like infections, allergies, and glaucoma.

  • Quality Control and Compliance: Rigorous quality assurance protocols and compliance with regulatory standards, ensuring the highest quality of ophthalmic products.

  • Customized Ophthalmic Solutions: Tailored development of ophthalmic products to meet specific therapeutic needs and patient requirements.


Your Trusted Partner in Ophthalmic Product Development

On Pharmaoffer, you can connect with CDMOs that are experts in the development and manufacturing of ophthalmic products. Our platform ensures you find the right partner capable of delivering high-quality, safe, and effective ocular treatments.

Powders and Granules

Powders and granules are versatile in pharmaceutical manufacturing, used for oral, topical, and reconstituted products. Their production involves careful particle size control and blending for uniformity, catering to a wide range of medical applications and dosage forms.


Pharmaoffer's selection of Contract Development and Manufacturing Organizations (CDMOs) includes experts in the production of powders and granules, versatile forms used in various pharmaceutical applications. These formulations are integral to oral, topical, and reconstituted pharmaceutical products, including those in Powders Dosage Form and Powder and Granules Manufacturing.


Key Services Provided by Our Listed CDMOs:


  • Particle Size Control: Precise control over particle size to ensure consistency, optimal absorption, and efficacy in various dosage forms. This is a critical aspect of Powder and Granules Manufacturing.

  • Uniform Blending Techniques: Advanced blending processes to ensure uniform distribution of active ingredients and excipients in powders and granules.

  • Flexible Formulation Capabilities: Development and manufacturing of powders and granules suitable for a wide range of medical applications, including customized formulations.

  • Quality Assurance and Compliance: Rigorous quality control measures and adherence to pharmaceutical manufacturing standards to ensure the safety and effectiveness of products.

  • Innovative Packaging Solutions: Provision of suitable packaging options to maintain product integrity and extend shelf life, ensuring ease of use for patients.


Find Your Powder and Granule Manufacturing Partner

Through Pharmaoffer, pharmaceutical professionals can connect with CDMOs that specialize in the development and manufacturing of powders and granules. Our platform ensures you find the right partner capable of delivering high-quality, versatile pharmaceutical formulations for diverse medical needs.

Salvat


Discover Salvat

Salvat is a global pharmaceutical company, specialized in the production of pharmaceuticals and provision of services as a contract development and manufacturing organization (CDMO). With a specialized focus on sterile liquids in single-dose vials, we are headquartered in Barcelona, Spain, and have a subsidiary in Miami, US.

Our reach extends to over 60 countries worldwide, where we develop, manufacture, and market a diverse range of pharmaceutical products across several therapeutic areas, including ophthalmology, otolaryngology, gastroenterology, and wound care. Through strategic global alliances, we continuously innovate and contribute to enhancing patient care.

 

Our comprehensive CDMO service solutions:

We provide end-to-end, fully integrated drug development and manufacturing solutions that adhere to the highest GMP & FDA standards. Our state-of-the-art facilities and advanced technologies enable us to deliver exceptional products, including:

  • Single-dose vials of sterile liquids using Blow-Fill-Seal technology (Rommelag technology). With 7 production lines (2 in Barcelona, 4 in Madrid and 1 in Florida), we can produce over 300M u/year, with fill volumes ranging from 0.20mL to 15mL and batch sizes ranging from 50L to 2000L.
  • Multi-dose bottles of sterile liquids using a bottle filling line (Groninger technology). We can produce over 25M u/year, with fill volumes ranging from 2mL to 15mL and batch sizes ranging from 100L to 2000L.
  • Multi-dose non-sterile liquids with batch sizes ranging from 50L to 2000L.
  • Solid dosage forms including tabletscapsules, and sachets. We have the capacity to produce over 195M u/year tablets, 100M u/year capsules, and 2.6M u/year sachets. Batch sizes for tablets and capsules range from 100kg to 500kg, while sachets range from 50kg to 250kg. We offer both coated and uncoated tablets, with full serialization and aggregation capabilities.

 

Partner with us

If you are interested in licensing our products or would like more information on how we can support the development and manufacturing of your product, please send us a message and we will get in touch with you.