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The Research Network

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Sandwich, GB

About The Research Network

The Research Network Ltd was founded in 2011 and provides Pharmaceutical R&D scientific consultancy, project management, outsourcing, training and due diligence services. Our experienced team has in depth expertise across the key drug discovery and development disciplines covering both small molecule and... Show more »

The Research Network Ltd was founded in 2011 and provides Pharmaceutical R&D scientific consultancy, project management, outsourcing, training and due diligence services. Our experienced team has in depth expertise across the key drug discovery and development disciplines covering both small molecule and biotherapeutics. We also collaborate with Universities and research organisations to progress new drug discovery ventures from lead identification through early clinical development.

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Our Services (34)


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Pharmaceutical Due Diligence

Price on request

For any company wishing to in-licence compounds or intellectual property from a third party, experts at The Research Network are available to conduct the necessary due diligence analysis required. We will ensure that the client receives objective and reliable information to enable them to make truly informed decisions.

Our TRN... Show more »

For any company wishing to in-licence compounds or intellectual property from a third party, experts at The Research Network are available to conduct the necessary due diligence analysis required. We will ensure that the client receives objective and reliable information to enable them to make truly informed decisions.

Our TRN team of consultants are able to offer:

  • Gap Analysis
  • Scientific review of non-clinical data packages (Pharmacology, Toxicology, ADME, CMC) for potential in-licensing of candidate drugs
  • Evaluation of the completeness of data package
  • Evaluation of the studies performed for regulatory compliance (Regulatory compliance analysis)
  • Critical assessment of any findings that may impact further development or regulatory compliance
  • Assessment of the relevance of findings to human safety
  • Strategic advice and guidance on additional studies to address findings or mitigate against the possibility of regulatory delays
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Scientific Sourcing

Price on request

Outsourcing pharmaceutical discovery and development activities offers the ability to maximiseresource and access a diverse range of services. Once the decision has been made to outsource an activity, the next challenge is to select the right CRO or service provider. This process can be overwhelming and time consuming.

The team... Show more »

Outsourcing pharmaceutical discovery and development activities offers the ability to maximiseresource and access a diverse range of services. Once the decision has been made to outsource an activity, the next challenge is to select the right CRO or service provider. This process can be overwhelming and time consuming.

The team at The Research Network has extensive knowledge of CROs and service providers across the globe, with particular expertise in India and China. Our industrial experience and independent view will help you find the solution that is right for you. Many CROs do outstanding work in certain research areas (e.g., compound synthesis) but may not have the required expertise in other areas such as protein supply, so at TRN our aim is to work with the most appropriate CRO to meet your specific request.

TRN does not represent CROs, but recommend those with a high performance, and we are driven to find the right partner to fit your project needs.

We can provide outsourcing solutions to one aspect of your research, or provide project management across a range of desired CROs for a program of drug discovery.
On your behalf, TRN will manage the Request for Quote process, liaise with suppliers to achieve the most competitive price and the most appropriate service model for you, e.g. on a fee for service, FTE, or combined basis.

Examples of research areas, where TRN can assist with your outsourcing needs are in:

  • Compound synthesis and supply
  • Library synthesis and supply
  • Medicinal chemistry projects including the delivery of test compounds
  • Protein Supply
  • In vitro and in vivo compound testing

Our consultants will project manage the work to ensure successful delivery and a positive outcome for any outsourced activity.

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Editorial and Writing Services

Price on request

We offer scientific journal writing and editing services across all disciplines of pharmaceutical research. Our team of writers, who are all native English speakers, have many years of experience in the pharmaceutical industry and have authored journal articles across a wide range of disciplines eg J Med Chem, Bioorg & Med Chem,... Show more »

We offer scientific journal writing and editing services across all disciplines of pharmaceutical research. Our team of writers, who are all native English speakers, have many years of experience in the pharmaceutical industry and have authored journal articles across a wide range of disciplines eg J Med Chem, Bioorg & Med Chem, Drug Discovery Today, Methods in Molecular Biology.

We understand the standards and expectations of journal editors, and apply our scientific writing and editing experience to the preparation of your documents.

We will work with you to create a professional scientific paper suitable for submission to the journal of your choice and based on the data available can make a recommendation of which journal would be the most appropriate. We will tailor the style of writing to meet the needs of your specific scientific journal and ensure that any data requirements are met.

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Patent Application Support

Price on request

In collaboration with our Network Partners from the fields of patent law and medicinal chemistry, The Research Network can help optimise your intellectual property through patent strategy, scope, example selection and compilation of experimental data packages. Together we offer a full medicinal chemistry patent service, or... Show more »

In collaboration with our Network Partners from the fields of patent law and medicinal chemistry, The Research Network can help optimise your intellectual property through patent strategy, scope, example selection and compilation of experimental data packages. Together we offer a full medicinal chemistry patent service, or individually, we can provide services to suit your specific need and budget. This provides a bespoke, cost-effective solution, to free your scientists whilst enhancing your intellectual property protection.

We offer patent support in the following areas:

  • Prior Art Review
  • Patent Strategy and Scope
  • Example Selection
  • Experimental Write-up and Data Packages
  • Chemistry and Pharmaceutical Attorney Expertise

Chemistry Patent Writing

The Research Network team has a wealth of expertise and experience in compiling chemistry patent data. Our team is comprised of inventors and authors of over 100 chemistry patents and publications. We can provide high quality, tailored, patent-ready Examples and Preparations, alongside General Methods sections. Our chemists are well practiced at condensing experimental write-ups and analysing data, helping you achieve optimum efficiency to meet the legal requirements of disclosure, whilst providing a cost-effective solution for future translations. Engaging The Research Network in writing and compiling both experimental and general methodology sections of your patent specifications allows your scientists more time to focus on key activities

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Medicinal Chemistry

Price on request

The Research Network (TRN) offers an expert Medicinal Chemistry design service to progress your drug discovery programs from initial target evaluation and hit identification (HI), through lead optimisation (LO) and to candidate drug (CD) selection. Compound design and quality are led by our Medicinal Chemistry team with in-depth... Show more »

The Research Network (TRN) offers an expert Medicinal Chemistry design service to progress your drug discovery programs from initial target evaluation and hit identification (HI), through lead optimisation (LO) and to candidate drug (CD) selection. Compound design and quality are led by our Medicinal Chemistry team with in-depth experience gained in both Pharma and Biotech R&D organisations.

We offer experience in Receptor, Enzyme, Peptide and Bio-conjugate drugs for oral, parenteral and inhaled delivery. Expert understanding of the properties to afford CDs with the desired PK profile and CMC characteristics. We advise on attrition with our in-house Attrition Knowledgebase, provide input into patent writing and Intellectual Property (IP) analysis and strategy.

With a wide range of expertise in our team of experienced medicinal chemists we are able to select the best expert for your needs and provide flexible scientific support as well as project management and leadership to your HI, LO and CD campaigns. We access a wide range of partner CRO’s to ensure the best-fit support for your project. Our experts cover many therapeutic areas: Cardiovascular; Metabolic Diseases; Respiratory; Inflammation; Oncology; Neuroscience; Dermatology and Virology; as well as large molecules approaches: Peptides and Bio-conjugation.

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Biology

Price on request

The TRN Biology team has over 70 years (collective) experience of working within the bio-pharmaceutical industry and academia to manage all aspects of biological research. Our team has extensive laboratory and leadership experience with numerous therapeutic areas including; oncology, pain, neuroscience, cardiovascular, respiratory... Show more »

The TRN Biology team has over 70 years (collective) experience of working within the bio-pharmaceutical industry and academia to manage all aspects of biological research. Our team has extensive laboratory and leadership experience with numerous therapeutic areas including; oncology, pain, neuroscience, cardiovascular, respiratory disease, immunology, genitourinary, sexual health, inflammation and infection.

We also have extensive experience of managing the logistics of global biological research, operating multinational/multisite collaborative research projects, ensuring delivery of results, analysis/interpretation of data and all necessary legal documentation is in place.

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Synthetic Chemistry

Price on request

The TRN Synthetic Chemistry Team specialise in providing expert support, consultancy, project management and design of bespoke solutions for your outsourcing research and synthethic strategy. We do not represent CROs but we are driven to finding the right partner to fit your project needs.

We deliver highly competitive quotes... Show more »

The TRN Synthetic Chemistry Team specialise in providing expert support, consultancy, project management and design of bespoke solutions for your outsourcing research and synthethic strategy. We do not represent CROs but we are driven to finding the right partner to fit your project needs.

We deliver highly competitive quotes and flexible resource options in all areas including the following:

FFS (Fee For Service) or FTE (Full Time Employee) requests to deliver:

  • Medicinal chemistry projects including the delivery of test compounds
  • Synthetic intermediates including monomers and templates to support parallel medicinal chemistry efforts
    Re-syntheses, metabolites, reference standards
  • Design of routes to difficult or speculative new chemistry
  • API delivery including custom syntheses, solid form analysis and formulation support
  • Bio conjugation strategy and synthesis

Parallel Medicinal Chemistry:

  • Using a preferred highly cost-effective expert supplier using extensive in-house file of monomers or using your own bespoke compounds and commercial reagents.

CRO Project Management:

  • Customised to meet the needs of the client, for one or multiple requests
  • CRO metrics
  • Cultural awareness, expertise working with India, China, America and Europe

Additional Services:

  • Route design and selection including optimising the link between discovery and early clinical development phases
  • Problem solving and technical trouble-shooting
  • Assistance with shipping, communication, data transfer, software solutions to support logistics
  • Import/Export logistics – Forms, HTS coding, couriers, customs
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Chemical Process Consulting

Price on request
  • Scale-up and production of leads and candidates for preclinical R&D, including IND-enabling tox batch
  • Selection of appropriate API physical form
  • Pharmaceutical salt screening, evaluation, selection and development
  • GMP manufacture to provide clinical API supply
  • Chemical process R&D – process optimization, process... Show more »
  • Scale-up and production of leads and candidates for preclinical R&D, including IND-enabling tox batch
  • Selection of appropriate API physical form
  • Pharmaceutical salt screening, evaluation, selection and development
  • GMP manufacture to provide clinical API supply
  • Chemical process R&D – process optimization, process discovery, asymmetric synthesis
  • Critical process impurity tracking and control
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Drug Development Project Management

Price on request
  • Application of expertise in the discovery and development new medicines
  • Developing program strategy options, which efficiently address needs and capitalise on opportunities
  • Building and delivering on effective plans, in line with individual client and compound needs
  • Facilitation of problem solving, decision analyses and... Show more »
  • Application of expertise in the discovery and development new medicines
  • Developing program strategy options, which efficiently address needs and capitalise on opportunities
  • Building and delivering on effective plans, in line with individual client and compound needs
  • Facilitation of problem solving, decision analyses and stakeholder management
  • Risk identification and development of mitigation strategies
  • Harmonising services to deliver key milestones
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Regulatory Affairs Services

Price on request

The TRN regulatory team can help with all aspect of your regulatory affairs from discovery to commercialization across all therapeutic areas. Our highly experienced team can help with:

  • Managing and optimizing communication with regulatory authorities, enabling clients to work more effectively and reducing time to... Show more »

The TRN regulatory team can help with all aspect of your regulatory affairs from discovery to commercialization across all therapeutic areas. Our highly experienced team can help with:

  • Managing and optimizing communication with regulatory authorities, enabling clients to work more effectively and reducing time to registration/marketing
  • Meeting your specific regulatory needs with global agencies. From getting human clinical trails started to registering new medicines, variations or updates to exiting ones
  • Submission management: Our team has a proven record in every aspect of global electronic and paper document preparation and assembly, including extensive expertise in compiling documentation to support clinical trials and registration dossiers.
  • Project leadership: we can help to ensure compliance with global regulations and enable the understanding and interpretation of the dynamic global regulatory landscape

Achieving Customer Goals

  • We can provide advice, consultancy and problem solving to enable:
  • IND / CTA filing for 1st in human studies
  • New drug / marketing authorisation applications

Why choose the TRN Regulatory team?

  • We have a team of experts who work cohesively together
  • We work in collaboration with trusted network partners and associates
  • We have individual experts with established blue chip credentials and SME experience
  • We can harness the benefits of big pharma expertise and matrixed teams
  • We have established good relationships with regulators
  • We can provide operational support of electronic filings
  • We are geographically and linguistically close to FDA, EMEA, HC and TGA
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GLP Study Monitoring

Price on request

The TRN Global Study Monitoring Team has extensive experience in the areas of: Toxicology, Safety Pharmacology, DMPK and Pathology. Located in the EU and US with strong connections in India and China, the team can help you by offering the following services:

What We Deliver

  • Scientific QC Review or reports & preparation... Show more »

The TRN Global Study Monitoring Team has extensive experience in the areas of: Toxicology, Safety Pharmacology, DMPK and Pathology. Located in the EU and US with strong connections in India and China, the team can help you by offering the following services:

What We Deliver

  • Scientific QC Review or reports & preparation of regulatory submission documentation
  • CRO selection
  • CRO auditing
  • Protocol design
  • Study Monitoring
  • Data review & QC
  • Pathology peer review (Board Certified)
  • Preparation and review of reports
  • Scientific review
  • Pathology review of reports
  • QA if needed via specialist CRO partners
  • Preparation and review of regulatory documentation

What is Unique About GSM?

  • Global presence and perspective
  • Integrated across key disciplines
  • Ability to rapidly deliver all aspects of project work
  • Single contract – rapid, flexible & cost effective response
  • Integrated study design, troubleshooting cross-discipline

Why Choose GSM?

Five reasons to choose GSM for your integrated study monitoring:

  1. Interactive team that will work with you to drive your project(s) forward
  • Extensive study monitoring expertise
  • Reduced travel and inconvenience
  • Study designs tailored to your needs
  • Global perspective and connections
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Histology and Pathology Services

Price on request
  • Toxicologic Pathology (study design, protocol review, study monitoring and necropsy supervision)
  • Pathology peer review and primary interpretation of gross, microscopic, and clinical pathology data from toxicology studies
  • Toxicological risk assessment and interaction with government regulatory authorities
  • Toxicologic Pathology (study design, protocol review, study monitoring and necropsy supervision)
  • Pathology peer review and primary interpretation of gross, microscopic, and clinical pathology data from toxicology studies
  • Toxicological risk assessment and interaction with government regulatory authorities
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Statistical Consulting

Price on request

The TRN statistics and decision support team can be engaged to optimize the value of your drug discovery program. Decision analysis enables project managers to identify the most efficient strategy to apply to an individual project, cluster of projects or portfolio.

Statistical expertise ensures the maximum information is... Show more »

The TRN statistics and decision support team can be engaged to optimize the value of your drug discovery program. Decision analysis enables project managers to identify the most efficient strategy to apply to an individual project, cluster of projects or portfolio.

Statistical expertise ensures the maximum information is obtained from experiments given the available resources and the resulting data is appropriately analysed to differentiate true signal from noise.

TRN can provide statistical expertise in the design and analysis of drug discovery projects. We have experienced, professional, statisticians who are used to working with scientists to achieve useable results with real data. We have experience in gene expression data, in vitro and in vivo pharmacology, and drug safety. We can provide practical solutions in all these areas through the effective application of statistical techniques. Services range from input into the planning of experiments, to enabling effective quality control, to identifying and implementing appropriate statistical methods for analysing experimental data and reporting the results. We can also provide extensive training and support for drug discovery scientists.

Examples of services provided include:

  • Sample size calculations for in vitro and in vivo experiments
  • Assay development and optimization using efficient DoE techniques.
  • Dose response analysis and EC50/IC50 determination.
  • Developing QC charts for process/assays control.
  • Analysis of gene expression data.
  • Analysis of designed experiments.
  • Programming statistical software (with particular expertise in R/Bioconductor programming).
  • Enabling implementation of the 3R’s with input into design, sample size calculations and analyses.
  • Training your scientists in statistical thinking and methods.

Examples of training we can provide:

  • Introductory statistics
  • Experimental design and analysis
  • Assay development
  • Design and analysis of dose response studies (including competitive antagonism and enzyme inhibition).

We understand that our clients’ needs vary and so our statistical support may take the form of advice or consultation; analysing your data; researching/developing techniques for a particular application or writing statistical programs for you to perform your own data analysis.

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Drug Development

Price on request

Drug Development Services

Drug Development Services

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Formulation Services

Price on request

Formulation & Manufacturing Services

Formulation & Manufacturing Services

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Project Management

Price on request

Project Management & Consulting Services

Project Management & Consulting Services

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Assay Development

Price on request

Experimental Design Services

Experimental Design Services

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Marketing, Communication & Graphic Design Services

Price on request

Marketing, Communication & Graphic Design Services

Marketing, Communication & Graphic Design Services

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Business Development, Marketing & Operations

Price on request

Business Development & Commercialization Services

Business Development & Commercialization Services

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Drug Discovery

Price on request

Drug Discovery Services

Drug Discovery Services

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Animal Model in vivo Analyses

Price on request

Animal Model in vivo Analyses Services

Animal Model in vivo Analyses Services

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Animal Imaging Consulting

Price on request
Request a quote for more information about this service.

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Biochemistry & Molecular Biology

Price on request

Biochemistry & Molecular Biology Services

Biochemistry & Molecular Biology Services

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Genomics Consulting

Price on request
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Omics

Price on request

Omics Services

Omics Services

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Proteomics Consulting

Price on request
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Pharmaceutical Formulation

Price on request

Pharmaceutical Formulation Consulting

  • Development of nonclinical toxicology formulations
  • Preformulation studies
  • Development, selection and production/manufacture of clinical formulations

Pharmaceutical Formulation Consulting

  • Development of nonclinical toxicology formulations
  • Preformulation studies
  • Development, selection and production/manufacture of clinical formulations
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Drug Preformulation

Price on request

Drug Preformulation Consultancy

  • Strategic sourcing of vendors to provide pre-formulation, formulation development and analytical solutions for pre-clinical, toxicological and clinical studies
  • Technical evaluation of early lead molecules to risk assess pharmaceutical delivery and development options
  • Project and... Show more »

Drug Preformulation Consultancy

  • Strategic sourcing of vendors to provide pre-formulation, formulation development and analytical solutions for pre-clinical, toxicological and clinical studies
  • Technical evaluation of early lead molecules to risk assess pharmaceutical delivery and development options
  • Project and relationship management
  • Developing and ensuring execution of work plans to deliver high quality results
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ADME/DMPK Studies

Drug Metabolism and Pharmacokinetics
Price on request

The TRN ADME/DMPK team utilise a wide network of established service providers to deliver support in the following areas to optimise the quality, cost and speed of collaborative research:

  • Access to a wide range of non-GLP and GLP ADME assays
  • Vendor identification/selection.
  • Service agreement/work order generation
    -... Show more »

The TRN ADME/DMPK team utilise a wide network of established service providers to deliver support in the following areas to optimise the quality, cost and speed of collaborative research:

  • Access to a wide range of non-GLP and GLP ADME assays
  • Vendor identification/selection.
  • Service agreement/work order generation
  • Negotiating competitive quotes, scheduling, prioritisation and deliverables (timelines and output required)
  • Study design expertise
  • Study placement support – from compound shipment to data upload
  • Information transfer (study, methods, compound)
  • Watson study generation
  • Scientific troubleshooting
  • Data transfer, review & storage (online services, Secure email, etc)
  • Timeline tracking
  • Market scan/research
  • Vendor audits and assessment (scientific and business)
  • Relationship management
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Safety Pharmacology

Price on request
  • Design and management of GLP-compliant safety pharmacology and supplemental safety pharmacology studies
  • Advice on potential target/mechanism related and compound safety pharmacology liabilities
  • Access to and interpretation of broad ligand profiling panels for assessing the potential to cause off-target effects
  • CRO... Show more »
  • Design and management of GLP-compliant safety pharmacology and supplemental safety pharmacology studies
  • Advice on potential target/mechanism related and compound safety pharmacology liabilities
  • Access to and interpretation of broad ligand profiling panels for assessing the potential to cause off-target effects
  • CRO selection, protocol design, study oversight, report review and subject matter expertise for outsourced studies
  • Preparation of regulatory documentsExtrapolation of safety pharmacology findings to man and assessment of risk/benefit
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Toxicology Consulting

Price on request
  • Design and management of toxicology studies including GLP compliance oversight
  • Investigative / supplemental toxicology tests
  • CRO selection
  • Protocol design, study oversight, report review and broad subject matter expertise for outsourced studies
  • Preparation of regulatory documents
  • Extrapolation of toxicology findings to man and assessment of risk/benefit
  • Design and management of toxicology studies including GLP compliance oversight
  • Investigative / supplemental toxicology tests
  • CRO selection
  • Protocol design, study oversight, report review and broad subject matter expertise for outsourced studies
  • Preparation of regulatory documents
  • Extrapolation of toxicology findings to man and assessment of risk/benefit
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Analytical Chemistry Services

Price on request

Analytical Chemistry Services

Analytical Chemistry Services

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Pharmacology

Price on request

Pharmacology Services

Pharmacology Services

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Toxicology

Price on request

Toxicology Services

Toxicology Services

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