Result for tag: "PAES"
Phase IV & RWE
Every research question is unique, and so is every study. TFS HealthScience works with you to select the best methodologies for your non-interventional and late phase studies. We access a variety of d...
clinical development services strategic resourcing phase 4 project management oncology clinical trials rare diseases managing through the crisis tfs groundbreaking discoveries bring solutions to market faster the tfs advantage phase ii clinical trial submission umbrella trial drugs retrospective ehealth quality and delivery co-monitorings qppv drug safety physician reliable data manuscript risk-based audits safety accountability clinical services outsourcing engaged and motivated leadership team as well as the project teams with a partnerhsip minded approach and customer centric focus. macular degradation parkinson’s disease cystic fibrosis fragile skin c-peptide patient engagement visual field test emetogenic chemotherapy maximum tolerated dose ocular disorders endocrinology neuroscience clinical development nursing healthscience strategic insourcing phase four resourcing solutions oncology clinical development orphan drug development seamless collaboration tfs innovations open minded professionals join a global company phase three clinical trial approval biosimilarity biologics database digital health project tracking project delivery gvp periodic reports robust procedures clinical evaluation report medical monitor assurance of gcp global outsourcing solutions dermatology trial retinopathy stroke veeva patient reported outcomes mixed meal tolerance test site engagement sd-optical coherence tomography chemotherapy-induced nausea and vomiting progressive multifocal leukoencephalopathy retinal disease metabolic pain clinical development health science workforce management rwe study recruitment services dermatology pediatric clinical development tfs healthscience insights tfs expert opinions team players multidisciplinary assignments phase iii study conduct bioequivalence devices pragmatic virtual studies expert data collection site level good pharmacovigilance practices safety management plan proficient teams abstract medical safety monitoring assure quality managed team full service cro retinopathies traumatic brain injury clinical suite registry metabolic disorders high screen failure multifocal electroretinography cinv pml data management and biostatistics respiratory analgesia life science phasei-iv outcomes trial individual resourcing immunology rwe tfs health science insights tfs results grow your professional role helpful teammates phase 3 protocol development pet imaging therapeutic development phase iv questionnaire project sop local level literature searching sdea preferred edc systems and in-house database programmers poster medical expertise senior study oversight contract teams atopic dermatitis trial keratocjunctivitis anxiety gene therapy tfs-rwe algorithm t1d ediary bcva site identification fumaric acid esters ophthalmology clinical development covid multiple sclerosis clinical workforce management real world evidence health economics insourcing inflammatory disease approach to covid-19 tfs case studies register for trials broad experience supportive mentors phase 2a first in man pharmacokinetics electronic data capture nis pharmacoeconomics project standard operating procedures site aggregate report safety data exchange agreement efficient management of protocol deviations inform consent physician oversight clinical integrity contract workforce psoriasis trial glaucoma chronic fatigue syndrome cell therapy digital trials teamwork investigational medicinal product vfq-25 site training faes ophthalmology expertise ear nose and throat schizophrenia oncology cro non-interventional studies real world outcomes workforce management solutions dermatology clinical development treatment options tfs white papers potential investigator opportunities to grow welcoming atmosphere phase 2b proof of concept pharmacodynamics edc cross-sectional clinical project management manage issues and risks sites dsur training cost-effective and flexible edc solutions study results posting medical data review clinical study expert contract clinical development eczema trial dry eye depression wound healing digital studies flexibility imp collaboration restrictive inclusion/exclusion monitoring regulations contractt research organization ent addiction hematology cro pragmatic phase 4 trials functional services provider fully managed teams internal medicine expertise current covid-19 studies tfs articles potential clinical site team environment working with experts phase iia micro dosing pk/pd clinical trial management system cohort partnership with customers clinical project plan principal investigator psur audit readiness ecoa internal tools quality study report review clinical trial guidance contracted clinical development prurigo nodularis trial corneal disorder insomnia genetic engineering immuno-oncology geriatric genetic engineering unit site activation colorectal monitoring rules rare disease nephrology sleep hemato-oncology cro virtual trials fsp flexible staffing investigator sites continuity of business tfs library of articles clinical trial registration family environment career assistance phase iib single ascending dose regulatory affairs strategy clinical data platform epro relationship of trust project communication study coordinator rmp inspection readiness expert biostatisticians gcp protocol design review assess inclusion exclusion contracted workforce clinical trial in dermatology diabetic macular oedema type 1 diabetes small molecule inhibitors i-o visual acuity genetically modified bacteria oct technician nsclc gastrointestinal symptoms real time edc urology connect clinical trials dermatology cro virtual clinical development fsp model end to end global clinical development men's and women's health studies mobilized resources and capabilities tfs resources involvment in clinical studies appreciated specialists challenging projects early phase unit sad bioanalytical virtual study pro quality performance study documentation site staff expedited reporting audit topline results audits site team interaction 24/7 study questions answers contracted cro dermatology study ocular inflammation colitis chronic skin disease biomarkers sd-oct fee negotiation european strategic action program ovarian flushing relationsheep women’s health network mid-size cro ophthamology cro tailored solutions regulatory and study start up outsourcing model cardiovascular clinical development flexible solutions tfs key opinion leaders planned clinical trial in immense job satisfaction grow together as a team clinical development journey mad pediatric virtual clinical trial coa adherence to timelines manage project closeout centralized monitoring xevmpd inspection cdisc mapping sops study design functional services cro outsourcing ophthalmology cro retinal vein occlusion crohn’s disease inflammed skin ethics tcr-t intravenous injection healthy volunteer pancreatic dsmb expert cro hypertension expert european cro neurology cro clinical development clinical monitoring solutions driven professionals delivering quality gastrointestinal clinical development new reality tfs kols database of clinical trials collaborative environment early phase product approval multiple ascending dose elderly rwd ecoa on time and on budget site management drug safety sae risk mitigation regulatory writing csv study close out outsourcing solutions fsp cro ophthalmology product development retinal dystrophy irritable bowel syndrome itchy skin toxicity cell immunotherapy inherited retinal disease vaccine gastric aiom/siapec certification ophthalmic clinical development acute coronary syndrome customer global cro rwe cro midsize cro