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In simple words, the power of cell therapeutics is in modifying/changing the structure of a patient's own cells from a viable donor in order to fight diseases and improve underlying health conditions.

At Mares Ltd, you gain access to solutions that are spread across cellular therapy, aseptic processing, consulting services and a wide range of advanced technologies.

On the other hand, the power of gene therapies in the medical field can empower the body's ability to fight diseases and restore equilibrium, which is scientifically proven.

Gene and cell therapeutic services at Mares can help mitigate medical complexities and pave the way for advanced technologies for state-of-the-art healthcare.

Innovation & Products

Macro-Scale Innovation & Products

The primary goal of innovation is to produce something extraordinary from the mundane.

Considering the impact of technology in the healthcare industry, Advanced Therapy or Advanced Therapy Medicinal Products are certain to change the game of how pharmaceuticals and hospitals operate.

At Mares, you are empowered with:

Process Development

Process Development & Interpretation

The Process Development phase includes collecting relevant evidence supporting a client/partner. Upon validating and reviewing the data, a manufacturing process is devised and agreed.

Furthermore, based on the results, Process Development steps are checked for reliability, robustness, approval and scalability.

At Mares, we ensure you are equipped with:

Aseptic Processes

Aseptic Processes & Designs

Aseptic Processing is the process of packaging a sterile product into sterilized containers to avoid microbiological contamination.

Here at Mares, based on the client's process and requirements, we design state-of-the-art manufacturing plants. Additionally, you can be rest assured about process transparency, flow of goods and monitoring environmental procedures.

Quality Processes & Designs

Quality Processes and Systems

Adhering to EU-GMP and PIC/S regulatory guidelines,
Mares Consulting offers quality systems that include:

Equipment Qualification

This involves:

Regulatory

Regulatory Compliance

Once an organization or an independent business group decides to produce a drug directed for human usage in the European Union, a manufacturing permit is mandatory.

This includes a full review of quality processes, manufacturing plant and relevant system documentation.

Furthermore, a QP or a Qualified Person is eligible and competent to release products.

Good news? Mares offers QP services so you don't look any further!

Macro-Scale Innovation & Products

The primary goal of innovation is to produce something extraordinary from the mundane.

Considering the impact of technology in the healthcare industry, Advanced Therapy or Advanced Therapy Medicinal Products are certain to change the game of how pharmaceuticals and hospitals operate.

At Mares, you are empowered with:

Process Development & Interpretation

The Process Development phase includes collecting relevant evidence supporting a client/partner. Upon validating and reviewing the data, a manufacturing process is devised and agreed.

Furthermore, based on the results, Process Development steps are checked for reliability, robustness, approval and scalability.

At Mares, we ensure you are equipped with:

Aseptic Processes & Designs

Aseptic Processing is the process of packaging a sterile product into sterilized containers to avoid microbiological contamination.

Here at Mares, based on the client's process and requirements, we design state-of-the-art manufacturing plants. Additionally, you can be rest assured about process transparency, flow of goods and monitoring environmental procedures.

mares images

Quality Processes and Systems

Adhering to EU-GMP and PIC/S regulatory guidelines,
Mares Consulting offers quality systems that include:

Equipment Qualification

This involves:

Regulatory Compliance

Once an organization or an independent business group decides to produce a drug directed for human usage in the European Union, a manufacturing permit is mandatory.

This includes a full review of quality processes, manufacturing plant and relevant system documentation.

Furthermore, a QP or a Qualified Person is eligible and competent to release products.

Good news? Mares offers QP services so you don't look any further!

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