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Geneticist Inc.

Glendale, California, US

Geneticist is a state-of-the-art provider of human tissue samples and clinical information of the highest quality standards.

Geneticist was established in 2009 as a privately held company in Los Angeles. We offer a paramount quality of specimens at our biorepository and a selective and specially crafted human tissue-based research administration, which is our organization's biggest and quickest developing business segment. Our extensive biorepository is developed with cutting edge technology because being absolutely state-of-the-art is a necessity for our company's future success and the advanced global research efforts we play a role in. We are proud to offer optimal services and clinical specimens including tissues, blood, serum, bone marrow, tissue microarrays and full access to our biorepository. Our specimens are gathered from a system of scholarly and proficient clinical foundations under strict moral... Show more »

Geneticist is a state-of-the-art provider of human tissue samples and clinical information of the highest quality standards.

Geneticist was established in 2009 as a privately held company in Los Angeles. We offer a paramount quality of specimens at our biorepository and a selective and specially crafted human tissue-based research administration, which is our organization's biggest and quickest developing business segment. Our extensive biorepository is developed with cutting edge technology because being absolutely state-of-the-art is a necessity for our company's future success and the advanced global research efforts we play a role in. We are proud to offer optimal services and clinical specimens including tissues, blood, serum, bone marrow, tissue microarrays and full access to our biorepository. Our specimens are gathered from a system of scholarly and proficient clinical foundations under strict moral gauge.

At Geneticist’s biorepository, we collect biomaterial from targets such as Dermatology, Oncology, Immunology, Infectious Diseases, Neurology, Autoimmune and Metabolic disorders. Our specimens are extracted utilizing the most humane and ethical practices from a wide variety of human sources supported by pathological information and the patient’s clinical and historical documentation.

Browse our Inventory:
http://www.geneticistinc.com/frozen-tissue-samples/

Relevant publications:
http://www.geneticistinc.com/blog/

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Geneticist Inc. has not listed any services.

Human Tissue Procurement
Price on request

FRESH FROZEN TISSUE SAMPLES

  • All fresh frozen tissue samples are collected under IRB approval by certified medical pathologists.
  • Standard sample weight is 0.5 – 1.0 gram.
  • Tissues are stored in vapor-phase liquid nitrogen (-190°C).
  • Frozen tissues are never allowed to thaw after initial freezing.
  • Any diseased... Show more »

FRESH FROZEN TISSUE SAMPLES

  • All fresh frozen tissue samples are collected under IRB approval by certified medical pathologists.
  • Standard sample weight is 0.5 – 1.0 gram.
  • Tissues are stored in vapor-phase liquid nitrogen (-190°C).
  • Frozen tissues are never allowed to thaw after initial freezing.
  • Any diseased tissue specimen may be individually ordered, or paired with its FFPE tissue or fluid sample (ie. blood or biofluid), or NAT (normal adjacent tissue)

FORMALIN-FIXED, PARAFFIN-EMBEDDED (FFPE) TISSUE BLOCKS

  • All formalin-fixed, paraffin-embedded (FFPE) tissue specimens are collected under IRB approval by certified medical pathologists.
  • Tissues are fixed in 10% Neutral-Buffered Formalin (NBF) within 30 minutes of surgery excision.
  • Tissues are fixed for 18 – 24 hours at room temperature, then embedded in IHC-grade paraffin.
  • Standard sample size is 1 x 1 x 0.5 cm, but can vary based on the nature of the disease or tissue type.
  • The fixation agent and embedding media can be customized upon request.
  • FFPE tissue samples are stored at room temperature.
  • Unless indicated, all FFPE tumor tissues have at least 50% tumor content.
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Human Biofluids
Price on request
  • Urine specimens can be collected from a large variety of normal and diseased donors,
  • All urine specimens are collected before any surgery, unless noted or requested otherwise.
  • Urine specimens are collected under IRB approval, following a strict SOP.
  • Urine specimens are frozen within 1 hour of collection and are stored... Show more »
  • Urine specimens can be collected from a large variety of normal and diseased donors,
  • All urine specimens are collected before any surgery, unless noted or requested otherwise.
  • Urine specimens are collected under IRB approval, following a strict SOP.
  • Urine specimens are frozen within 1 hour of collection and are stored at -80°C.

Urine is not regularly collected for storage in our stock, but we can easily set up a prospective collection customized to our customers’ specifications.

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Human Whole Blood
Price on request
  • Blood products are collected from a wide range of clinical conditions.
  • can collect up to 40 mL of whole blood per donor.
  • All blood products are kept frozen and never allowed to thaw.
  • can also provide buffy coat specimens pulled from fractionated blood.
  • We can also provide whole blood with matching Fresh Frozen and/or... Show more »
  • Blood products are collected from a wide range of clinical conditions.
  • can collect up to 40 mL of whole blood per donor.
  • All blood products are kept frozen and never allowed to thaw.
  • can also provide buffy coat specimens pulled from fractionated blood.
  • We can also provide whole blood with matching Fresh Frozen and/or FFPE Tissues.
  • Whole blood is not collected for regular storage in our Biorepository, but we can easily set up a Custom Collection to meet our customers’ needs.
  • Whole blood can be collected in a variety of test tubes such as:
    • K2- or K3-EDTA tubes
    • SST tubes
    • Sodium (Na) or Lithium (Li) Heparin tubes
    • Sodium (Na) Citrate tubes
    • PAXgene RNA and DNA tubes
    • CPT tubes
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Quality Assurance
Price on request
  • Evaluation of Standard Operating Procedures and Study Specific Procedures for their consistency with International Quality Standards for designing, conducting, recording, and reporting clinical trials (ICH guidelines)
  • Assistance to Functional Managers in the development of Standard Operating Procedures
  • Approval of all... Show more »
  • Evaluation of Standard Operating Procedures and Study Specific Procedures for their consistency with International Quality Standards for designing, conducting, recording, and reporting clinical trials (ICH guidelines)
  • Assistance to Functional Managers in the development of Standard Operating Procedures
  • Approval of all Standard Operating Procedures and monitoring of the development, approval, periodic review, revision, version control, and historical archival of all Standard Operating Procedures
  • Conducting of Internal Audits to ensure that operation of all Functional Groups is in compliance with the internal Standard Operating Procedures
  • Overseeing external auditing or vendor qualification function (per Sponsor request)
  • Preparations for inspections by Sponsor and Regulatory Authorities
  • Representation of Sponsor in interactions with external organizations including Regulatory Authorities, Clinical Trial sites, and other organizations
  • Serving as a primary contact during all audits
  • Generation of responses to audit reports
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Regulatory Affairs Consulting
Price on request
  • Regulatory submission for approval of Department of Health
  • Regulatory submission for approval of Pharmacology Committee and National Ethics Committee
  • Obtaining of Import/Export Licenses
  • Expedited Study Approvals
  • Local Insurance policies for patients
  • Regulatory submission for approval of Department of Health
  • Regulatory submission for approval of Pharmacology Committee and National Ethics Committee
  • Obtaining of Import/Export Licenses
  • Expedited Study Approvals
  • Local Insurance policies for patients
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Biostatistical Analysis
Price on request
  • Statistical consulting
  • Sample size estimation
  • Randomization
  • Analysis plans
  • Statistical analysis
  • Statistical writing
  • Presentation of results
  • Statistical consulting
  • Sample size estimation
  • Randomization
  • Analysis plans
  • Statistical analysis
  • Statistical writing
  • Presentation of results
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Data Management
Price on request
  • Data entry & verification
  • Data validation & query management
  • CRF & query tracking
  • Coding of diseases & medications
  • Import & export data
  • Presentation of results
  • Data entry & verification
  • Data validation & query management
  • CRF & query tracking
  • Coding of diseases & medications
  • Import & export data
  • Presentation of results
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Tissue Microarrays
Price on request

Customized tissue microarrays could be utilized to corroborate clinical pertinence of potential bio-targets in the advancement of therapeutics, diagnostics, and in considering new protein markers and genes. Geneticist gives customized tissue microarrays or also called (TMAs) for target definition and biomarker investigation in... Show more »

Customized tissue microarrays could be utilized to corroborate clinical pertinence of potential bio-targets in the advancement of therapeutics, diagnostics, and in considering new protein markers and genes. Geneticist gives customized tissue microarrays or also called (TMAs) for target definition and biomarker investigation in ordinary adjoining, infected, and normal tissues. The utilization of TMAs offers an optional quality control system for non-research applications as well.

Geneticist constructs tissue microarrays utilizing precisely chosen donors. Definite tissue confinement in every TMA unit is recorded with extreme precision by our geneticists. Please contact us to find out more about our customized tissue microarrays.

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Pharmacovigilance and Post-Authorization Safety Studies
Price on request
  • SAE training of clinical personnel
  • Creation of study-specific SAE reporting Standard Operating Procedures
  • SAE reporting and Sponsor notifications (24 hours 7 days a week)
  • Preparation and submission of SAE reports to Regulatory Authorities, Investigators, and to local Ethics Committees
  • Generation of SAE narratives and follow-up reports, translation of medical records
  • SAE training of clinical personnel
  • Creation of study-specific SAE reporting Standard Operating Procedures
  • SAE reporting and Sponsor notifications (24 hours 7 days a week)
  • Preparation and submission of SAE reports to Regulatory Authorities, Investigators, and to local Ethics Committees
  • Generation of SAE narratives and follow-up reports, translation of medical records
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Clinical Trial Management
Price on request
  • On-site personnel training
  • On-site monitoring (pre-study, initiation, interim and close-out visits)
  • In-house site management, CRF review
  • Regulatory documents collection and review
  • Monitoring of regulatory status of studies on sites
  • Management of information collection from Investigational site
  • Monitoring... Show more »
  • On-site personnel training
  • On-site monitoring (pre-study, initiation, interim and close-out visits)
  • In-house site management, CRF review
  • Regulatory documents collection and review
  • Monitoring of regulatory status of studies on sites
  • Management of information collection from Investigational site
  • Monitoring reports completion
  • Query resolution
  • Participation in Investigators meetings
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Project Management
Price on request
  • developing and maintaining study plan and timelines
  • communicating study expectations to team members
  • provisioning study-specific training for CRAs
  • study budget preparation
  • preparing meetings with agendas and minutes
  • preparing enrollment notification and updates, site newsletters, study updates, protocol deviations, etc.
  • developing and maintaining study plan and timelines
  • communicating study expectations to team members
  • provisioning study-specific training for CRAs
  • study budget preparation
  • preparing meetings with agendas and minutes
  • preparing enrollment notification and updates, site newsletters, study updates, protocol deviations, etc.
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Biospecimens
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Computational Modeling
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Clinical Trials, Consulting, and Management
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Regulatory Affairs Services
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Product Development, Testing, and Packaging
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Biochemistry & Molecular Biology
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Product Quality Control
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Protein Expression Visualization
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Clinical Research
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Cells and Tissues
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Human Biospecimen Collection
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Biostatistics & Bioinformatics
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Data Services
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Human Biospecimens
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Process Consulting
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Protein Services
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Human Whole Blood & PBMCs
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Biology
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