Toxlicon range of services
We offer comprehensive services in individual test support, the management of complex projects and scientific consulting. Our focus is on the development of test strategies for regulatory approvals, laboratory commissioning and independent study monitoring.
Our expertise covers numerous product groups, including chemicals, agrochemicals, biocides, pesticides, pharmaceuticals, medical devices, veterinary pharmaceuticals, animal feed and food.
We cover ingredients, reaction products and mixtures. Within various authorisation frameworks, we offer tests according to REACH (GLP/non-GLP), EFSA and EMA approvals, as well as environmental risk assessments (ERA) for human and veterinary medicinal products.
We also provide support for SVHC tests and authorisation tests according to ISO standards, for example for medical devices (MDR).
Get advice nowWe cover ingredients, reaction products and mixtures. Within various authorisation frameworks, we offer tests according to REACH (GLP/non-GLP), EFSA and EMA approvals, as well as environmental risk assessments (ERA) for human and veterinary medicinal products.
We also provide support for SVHC tests and authorisation tests according to ISO standards, for example for medical devices (MDR).
Find out more about our services
We offer a comprehensive range of services that includes scientific and regulatory consulting, the development of test strategies for regulatory approvals, test and project support and the commissioning of laboratories.
We also provide support with professional study monitoring for GLP studies and the preparation of complete authorisation dossiers. Our services can be flexibly tailored to your needs, either individually or as a customised package.
We also provide support with professional study monitoring for GLP studies and the preparation of complete authorisation dossiers. Our services can be flexibly tailored to your needs, either individually or as a customised package.
Scientific and regulatory advice
Test strategy for regulatory approval
Test and project support
Laboratory commissioning
Study monitoring of GLP studies
Dossier creation
Toxlicon converts your requirements into a test strategy exclusively with the placement of necessary laboratory tests for your product safety.
- Customer-oriented
- Scientifically and toxicologically highly qualified
- Flexible
- Personally
Scientific and regulatory advice
Expertise for safe decisions
We are your reliable partner for scientific and regulatory advice. With in-depth expertise and a clear understanding of the complex legal requirements (e.g. REACH, FDA, EMA), we guide you through every step of the authorisation process. We help you to implement regulatory requirements precisely and to design your study in such a way that it fulfils the highest scientific and legal standards.
Our advice is based on a personal and trusting approach. We work closely with you to develop customised solutions that are tailored to the needs of your project. We help you to understand and correctly evaluate toxicological data and thus create the basis for a successful and sustainable authorisation of your product.
Feel free to contact us to organise your testing strategy in an efficient and targeted manner.
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Test strategy for regulatory approval
Safely to market approval
For the regulatory approval of your products, we develop customized test strategies that ensure that all required toxicological data is generated reliably and accurately.
Our approach includes the selection of suitable tests, the definition of dose and test conditions and the creation of a clearly structured schedule for conducting the studies. In addition, we ensure 3Rs-compliant planning, conduct and monitoring of animal studies, with a particular focus on animal welfare and the avoidance of animal studies wherever possible on a state-of-the-art scale. We always keep an eye on regulatory requirements and the highest current scientific standards in order to optimally support the approval process.
With our expertise and a comprehensive understanding of the legal requirements and the latest laboratory technology options, we can help you to overcome complex challenges and bring your product to market safely and efficiently.
Let’s work together to perfect your approval strategy – get in touch!
Test and project support
Individual, personal and tailor-made
Every project that we supervise is important and valuable to us and we accompany it individually with the greatest care.
Our commitment includes the coordination between clients, laboratories and test centres. We ensure that all studies are planned efficiently, carried out smoothly and documented seamlessly. Our personalised and reliable support ensures that your project not only complies with regulatory standards, but also meets your individual expectations.
Entrust us with your project - we will take care of it with passion and precision.
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Laboratory commissioning
Many years of experience ensure the highest quality
Choosing the right laboratory is a crucial step for the success of toxicology testing - we support you with our experience and our extensive international network.Thanks to our in-depth knowledge of the strengths and weaknesses of laboratories, we can help you find the facility that best suits your project.
Our focus is on ensuring that the laboratories not only have the necessary experience and accreditations, but that they also carry out your studies reliably and in accordance with all applicable regulations and deliver reliable results.It is important to us that the Supply Chain Duty of Care Act is complied with in the best possible way:Transparency, integrity and responsibility are values that we expect from our partner laboratories as much as from ourselves. We ensure that ethical standards, fair working conditions and sustainable business practices form the basis of our collaboration.
As close and personal cooperation is important to us, we visit our laboratories regularly. In this way, we not only guarantee reliable results, but also a trusting partnership that meets your requirements in the best possible way.
Rely on a trusting collaboration - together we will find the perfect laboratory for your studies.
Get advice nowOur focus is on ensuring that the laboratories not only have the necessary experience and accreditations, but that they also carry out your studies reliably and in accordance with all applicable regulations and deliver reliable results.It is important to us that the Supply Chain Duty of Care Act is complied with in the best possible way:Transparency, integrity and responsibility are values that we expect from our partner laboratories as much as from ourselves. We ensure that ethical standards, fair working conditions and sustainable business practices form the basis of our collaboration.
As close and personal cooperation is important to us, we visit our laboratories regularly. In this way, we not only guarantee reliable results, but also a trusting partnership that meets your requirements in the best possible way.
Rely on a trusting collaboration - together we will find the perfect laboratory for your studies.
Study monitoring of GLP studies
Scientific expertise that pays off
With a clear focus on quality and precision, we monitor all phases of the studies and ensure that they meet the highest scientific standards. Our scientific expertise ensures that your GLP (Good Laboratory Practice) studies run smoothly and to the highest technical standards.
We review study plans and reports for completeness and compliance, check data integrity and ensure that all GLP guidelines are fully adhered to. Our monitoring gives you the assurance that your studies not only fulfil regulatory requirements, but also deliver reliable and robust results with the highest scientific significance.
You can rely on our expertise - for state-of-the-art studies that are scientifically sound and perfectly controlled.
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Dossier creation
With expertise for rapid official acceptance
The preparation of a convincing registration dossier is the key to a successful and efficient regulatory authorisation. We take responsibility for preparing comprehensive dossiers that fully and accurately summarise all necessary toxicological data and study results.
With our experience, we coordinate the compilation of relevant studies and ensure that all documents comply with regulatory requirements and that the information can be easily submitted to ECHA in the appropriate IUCLID format. Our aim is to design your dossier so that it is quickly accepted by the relevant authority and the authorisation process runs smoothly.
Put your trust in our expertise - for dossiers that are convincing and deliver reliable results.
Get advice now3R principles
The 3-R principles (Replacement, Reduction, Refinement) are ethical guidelines for improving animal research, where the three “Rs” stand for:
Replacement:Animal testing should, as far as possible, be replaced by alternative methods, such as in vitro tests or computerised models.
Reduction:The number of animals used should be reduced to the minimum necessary to achieve meaningful results.
Refinement (streamlining): Animal experiments that are required by the authorities should be optimised in such a way that the stress on the animals is minimised, for example through less invasive procedures or improved care and accommodation.
These principles should contribute to this.
We strictly adhere to the 3-R principles (Replacement, Reduction, Refinement) and are actively committed to minimizing the use of animals in research while ensuring scientifically sound and reliable results, and to continuously expand and implement this approach in the interests of animal welfare. We constantly strive to replace animal testing with innovative alternatives, to reduce the use of animals to the necessary minimum and to refine existing methods so that the burden on animals is kept to an absolute minimum. Our aim is to maintain the highest ethical standards and consistently meet animal welfare requirements in order to achieve results that are both scientifically sound and in line with animal welfare standards.
Your personal contact
Your personal contact partners will accompany you from the initial inquiry through to implementation and ensure fast, individual solutions.
- + 49 30 843 13 661
- info@toxlicon.com