EN
EN

Analytical Services

Analytical Services

Analytical Services

Analytical Services

Provision of Advanced Analytical Services

Analytical excellence with international standard infrastructure

The largest analytical park in Latin America for mass spectrometry

We conduct advanced analyses with high precision and traceability, supported by a robust LC-MS/MS park and state-of-the-art chromatographic and physicochemical techniques.

We meet the requirements of ANVISA, FDA, and EMA, ensuring consistent methods, accurate timelines, and reliable data for development, registration, and quality control.

Our solutions

For recurring demands or specific projects, our solutions offer the precision, flexibility, and reliability needed to support the development and registration of medications.

Development & Validation of Methods

Method Development and Validation

Deformulation

Compatibility

Solubility

Impurities & Chemical Risks

Elementary Impurities

Nitrite (in excipient)

Nitrosamines (Phase I and II)

Extractable and Leachable (Phase I and II)

Characterization & Special Studies

Characterization of Substances

Particle Size and Morphology

Polymorphism

Organic Prediction and Forced Degradation

Processes & Compliance

Cleaning Validation

Process Validation

Compatibility

Supplements (Vitamins and Minerals)

Development & Validation of Methods

Method Development and Validation

Deformulation

Compatibility

Solubility

Impurities & Chemical Risks

Elementary Impurities

Nitrite (in excipient)

Nitrosamines (Phase I and II)

Extractable and Leachable (Phase I and II)

Characterization & Special Studies

Characterization of Substances

Particle Size and Morphology

Polymorphism

Organic Prediction and Forced Degradation

Processes & Compliance

Cleaning Validation

Process Validation

Compatibility

Supplements (Vitamins and Minerals)

Development & Validation of Methods

Method Development and Validation

Deformulation

Compatibility

Solubility

Impurities & Chemical Risks

Elementary Impurities

Nitrite (in excipient)

Nitrosamines (Phase I and II)

Extractable and Leachable (Phase I and II)

Characterization & Special Studies

Characterization of Substances

Particle Size and Morphology

Polymorphism

Organic Prediction and Forced Degradation

Processes & Compliance

Cleaning Validation

Process Validation

Compatibility

Supplements (Vitamins and Minerals)

Development & Validation of Methods

Method Development and Validation

Deformulation

Compatibility

Solubility

Impurities & Chemical Risks

Elementary Impurities

Nitrite (in excipient)

Nitrosamines (Phase I and II)

Extractable and Leachable (Phase I and II)

Characterization & Special Studies

Characterization of Substances

Particle Size and Morphology

Polymorphism

Organic Prediction and Forced Degradation

Processes & Compliance

Cleaning Validation

Process Validation

Compatibility

Supplements (Vitamins and Minerals)

Quality Control

We carry out physicochemical and microbiological analyses with technical rigor and complete traceability, ensuring that raw materials, intermediates, and final products meet the standards required by the main global regulations.

Physical-Chemical:

Theory, impurities, dissolution, hardness, moisture, purity, spectroscopy, and others.

Physical-Chemical:

Theory, impurities, dissolution, hardness, moisture, purity, spectroscopy, and others.

Physical-Chemical:

Theory, impurities, dissolution, hardness, moisture, purity, spectroscopy, and others.

Physical-Chemical:

Theory, impurities, dissolution, hardness, moisture, purity, spectroscopy, and others.

Microbiology:

Total count, pathogens, endotoxins, sterility, and analyses applied to pharmaceuticals, inputs, and supplements.

Microbiology:

Total count, pathogens, endotoxins, sterility, and analyses applied to pharmaceuticals, inputs, and supplements.

Microbiology:

Total count, pathogens, endotoxins, sterility, and analyses applied to pharmaceuticals, inputs, and supplements.

Microbiology:

Total count, pathogens, endotoxins, sterility, and analyses applied to pharmaceuticals, inputs, and supplements.

The largest analytical park in Latin America for mass spectrometry

Our modern facilities include state-of-the-art equipment, such as:

+30 LC-MS/MS

+30 LC-MS/MS

+30 LC-MS/MS

+30 LC-MS/MS

+25 LC-DAD

+25 LC-DAD

+25 LC-DAD

+25 LC-DAD

GC-FID

GC-FID

GC-FID

GC-FID

Antidiabetics

Antidiabetics

Antidiabetics

Antidiabetics

GC-MS/MS

GC-MS/MS

GC-MS/MS

GC-MS/MS

ICP-OES

ICP-OES

ICP-OES

ICP-OES

Validated infrastructure and global compliance

Our facilities meet international quality and safety standards, ensuring the credibility of every result delivered.

ANVISA
ANVISA
ANVISA
ANVISA
EMA
EMA
EMA
EMA
FDA
FDA
FDA
FDA
GCC
GCC
GCC
GCC

Harmonized studies

One single protocol, multiple countries

We operate in Latin America, Europe, and Gulf countries, conducting projects with a global standard of quality and compliance.

ICH–COFEPRIS–ANVISA aligned protocols

ICH–COFEPRIS–ANVISA aligned protocols

Trilingual documentation (PT, EN, and ES)

Trilingual documentation (PT, EN, and ES)

Management of import and export of samples

Management of import and export of samples

Experience with ANVISA, EMA, and FDA

Experience with ANVISA, EMA, and FDA

Harmonized studies

One single protocol, multiple countries

We operate in Latin America, Europe, and Gulf countries, conducting projects with a global standard of quality and compliance.

ICH–COFEPRIS–ANVISA aligned protocols

Trilingual documentation (PT, EN, and ES)

Management of import and export of samples

Experience with ANVISA, EMA, and FDA

Harmonized studies

One single protocol, multiple countries

We operate in Latin America, Europe, and Gulf countries, conducting projects with a global standard of quality and compliance.

ICH–COFEPRIS–ANVISA aligned protocols

Trilingual documentation (PT, EN, and ES)

Management of import and export of samples

Experience with ANVISA, EMA, and FDA

Excellence at every stage of study

From feasibility to final delivery, our technical and operational areas work together to ensure quality, agility, and full regulatory compliance.

Feasibility of projects

Feasibility of projects

Feasibility of projects

Feasibility of projects

History of the Center

History of the Center

History of the Center

History of the Center

Clinical stage

Clinical stage

Clinical stage

Clinical stage

Bioanalytical stage

Bioanalytical stage

Bioanalytical stage

Bioanalytical stage

Contact

Talk to our experts

Discover how Synvia can support your studies, analyses, and projects.

Contact

Talk to our experts

Discover how Synvia can support your studies, analyses, and projects.