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Approvals - Accreditations/ Certifications

Cambodia

Ethiopia

Kenya

Malawi

Nigeria

Sri Lanka

Sudan (Cosmetic products)

Sudan (Medical devices)

WHO-GMP Certification

Yemen

European Union (EU) Market

CE certified product

ISO 13485:2016 Certification

Represents a laboratory

Brassica Pharma takes great pride in the dedicated Formulation and Development (F&D) facilities that serve as a testament to our commitment to pharmaceutical excellence. Our F&D facility consists of a laboratory equipped with the latest technology and staffed by a team of highly skilled employees. It serves as the creative hub where innovation and customization are given wings. From the initial stages of lab-scale experiments to the production of pilot batches, our F&D facility provides a seamless continuum of pharmaceutical development.

This unique capability positions us as an invaluable partner to our clients, as it allows us to craft tailored pharmaceutical formulations that precisely align with their specific needs. Whether it’s optimizing an existing product, developing a new formulation, or addressing particular challenges, our F&D facility is the driving force behind innovative solutions. We are more than a pharmaceutical manufacturer; we are a partner in your success, dedicated to transforming ideas into tangible, market-ready pharmaceutical solutions. At Brassica Pharma, we offer not just products but a collaborative journey of pharmaceutical development, all backed by the expertise and innovation housed within our exceptional Formulation and Development facility.

Represents a laboratory

Brassica Pharma takes great pride in the dedicated Formulation and Development (F&D) facilities that serve as a testament to our commitment to pharmaceutical excellence. Our F&D facility consists of a laboratory equipped with the latest technology and staffed by a team of highly skilled employees. It serves as the creative hub where innovation and customization are given wings. From the initial stages of lab-scale experiments to the production of pilot batches, our F&D facility provides a seamless continuum of pharmaceutical development.

This unique capability positions us as an invaluable partner to our clients, as it allows us to craft tailored pharmaceutical formulations that precisely align with their specific needs. Whether it’s optimizing an existing product, developing a new formulation, or addressing particular challenges, our F&D facility is the driving force behind innovative solutions. We are more than a pharmaceutical manufacturer; we are a partner in your success, dedicated to transforming ideas into tangible, market-ready pharmaceutical solutions. At Brassica Pharma, we offer not just products but a collaborative journey of pharmaceutical development, all backed by the expertise and innovation housed within our exceptional Formulation and Development facility.

Manufacturing Capacity

Quality

At Brassica Pharma, our unwavering commitment to quality is reflected in the robust Quality Control and Quality Assurance system that underpins every facet of our pharmaceutical manufacturing. We place paramount importance on the integrity of our products and this starts with the validation of Master Formulae for all our formulations. These master formulae serve as the blueprint for the production of pharmaceuticals, ensuring that each ingredient is measured and combined with precision. Our systematic implementation of Standard Operating Procedures (SOPs) further reinforces the consistency and reliability of our manufacturing processes, guaranteeing that each product adheres to the highest quality standards.

Our dedication to quality doesn’t stop there. We conduct regular self-inspections to proactively identify and address any potential issues, ensuring that our manufacturing environment is in compliance with the most stringent standards. The rigorous implementation of Current Good Manufacturing Practices (cGMP) is a cornerstone of our operations, with every step of production meticulously monitored and controlled to meet regulatory requirements. As a result, our Quality Control processes go beyond routine checks; they are the guardians of product quality. With stringent measures in place, our customers trusts that Brassica Pharma consistently delivers high-quality finished pharmaceutical products that are not just effective but also safe and reliable.

EHS

At Brassica Pharma we are steadfast in our commitment to environmental stewardship and the health and safety of our employees, partners and the communities we serve. Our EHS policy forms the cornerstone of our operations, ensuring that we not only meet but exceed the highest industry standards. We understand the profound impact pharmaceutical manufacturing can have on the environment and, consequently, have implemented stringent measures to minimize our ecological footprint. From responsible waste management to the conservation of resources, we are dedicated to sustainable practices that safeguard our planet for future generations.

Equally vital is the health and safety of our workforce. Our EHS policy prioritizes the well-being of our employees, ensuring that every individual in our organization is provided with a safe and healthy working environment. This commitment extends to our peoples and the broader community, as we continuously work to minimize risks and mitigate potential hazards. At Brassica Pharma, our EHS policy is not just a compliance requirement but a guiding principle that reflects our responsibility to both people and the planet. We pledge to consistently improve and innovate our EHS practices, embracing the latest technologies and best practices to maintain our position as a trusted pharmaceutical manufacturer known for our unwavering commitment to EHS excellence.

EHS

At Brassica Pharma we are steadfast in our commitment to environmental stewardship and the health and safety of our employees, partners and the communities we serve. Our EHS policy forms the cornerstone of our operations, ensuring that we not only meet but exceed the highest industry standards. We understand the profound impact pharmaceutical manufacturing can have on the environment and, consequently, have implemented stringent measures to minimize our ecological footprint. From responsible waste management to the conservation of resources, we are dedicated to sustainable practices that safeguard our planet for future generations.

Equally vital is the health and safety of our workforce. Our EHS policy prioritizes the well-being of our employees, ensuring that every individual in our organization is provided with a safe and healthy working environment. This commitment extends to our peoples and the broader community, as we continuously work to minimize risks and mitigate potential hazards. At Brassica Pharma, our EHS policy is not just a compliance requirement but a guiding principle that reflects our responsibility to both people and the planet. We pledge to consistently improve and innovate our EHS practices, embracing the latest technologies and best practices to maintain our position as a trusted pharmaceutical manufacturer known for our unwavering commitment to EHS excellence.

Regulatory Affairs

At Brassica Pharma, we consider our Regulatory Affairs team as a vital conduit to accessing new markets. Our ongoing commitment to investing in this specialized team has yielded significant results in the form of increased product registrations on a global scale, serving as a catalyst for our continued growth.

Our Regulatory Affairs team comprises highly skilled and seasoned professionals who play a pivotal role in guiding drug development strategies within the constantly evolving pharmaceutical landscape. Comprised of experienced pharmacists with deep industry knowledge, they are dedicated to seamlessly integrating regulatory principles into our processes. This includes the meticulous preparation and submission of regulatory dossiers to health authorities. We also have a dedicated Liaison team. They vigilantly monitor the dynamic regulatory landscape, ensuring that our procedures and documentation consistently align with country-specific guidelines, thus maintaining the highest level of compliance.

Manufacturing Location