Class information for: |
Basic class information |
| ID | Publications | Average number of references |
Avg. shr. active ref. in WoS |
|---|---|---|---|
| 18530 | 482 | 22.3 | 37% |
Classes in level above (level 2) |
| ID, lev. above |
Publications | Label for level above |
|---|---|---|
| 1294 | 8163 | FOOD AND DRUG LAW JOURNAL//GENERIC SUBSTITUTION//DIRECT TO CONSUMER ADVERTISING |
Terms with highest relevance score |
| Rank | Term | Type of term | Relevance score (tfidf) |
Class's shr. of term's tot. occurrences |
Shr. of publ. in class containing term |
Num. of publ. in class |
|---|---|---|---|---|---|---|
| 1 | DRUG LAG | Author keyword | 13 | 67% | 2% | 12 |
| 2 | OFF PHARMACEUT IND | Address | 9 | 83% | 1% | 5 |
| 3 | JAPANESE CLINICAL TRIALS | Author keyword | 6 | 100% | 1% | 4 |
| 4 | STUDY DRUG DEV | Address | 4 | 31% | 2% | 11 |
| 5 | PHARMACEUT REGULATORY SCI | Address | 4 | 38% | 2% | 8 |
| 6 | APPROVAL TIMES | Author keyword | 3 | 100% | 1% | 3 |
| 7 | CLIN TRIAL GUIDANCE | Address | 3 | 100% | 1% | 3 |
| 8 | LABEL CHANGES | Author keyword | 3 | 100% | 1% | 3 |
| 9 | PRESCRIPTION DRUG USER FEE ACT OF 1992 | Author keyword | 3 | 100% | 1% | 3 |
| 10 | REVIEW AUDIT | Address | 3 | 100% | 1% | 3 |
Web of Science journal categories |
Author Key Words |
| Rank | Web of Science journal category | Relevance score (tfidf) |
Class's shr. of term's tot. occurrences |
Shr. of publ. in class containing term |
Num. of publ. in class |
LCSH search | Wikipedia search |
|---|---|---|---|---|---|---|---|
| 1 | DRUG LAG | 13 | 67% | 2% | 12 | Search DRUG+LAG | Search DRUG+LAG |
| 2 | JAPANESE CLINICAL TRIALS | 6 | 100% | 1% | 4 | Search JAPANESE+CLINICAL+TRIALS | Search JAPANESE+CLINICAL+TRIALS |
| 3 | APPROVAL TIMES | 3 | 100% | 1% | 3 | Search APPROVAL+TIMES | Search APPROVAL+TIMES |
| 4 | LABEL CHANGES | 3 | 100% | 1% | 3 | Search LABEL+CHANGES | Search LABEL+CHANGES |
| 5 | PRESCRIPTION DRUG USER FEE ACT OF 1992 | 3 | 100% | 1% | 3 | Search PRESCRIPTION+DRUG+USER+FEE+ACT+OF+1992 | Search PRESCRIPTION+DRUG+USER+FEE+ACT+OF+1992 |
| 6 | PRIORITY REVIEW | 3 | 50% | 1% | 4 | Search PRIORITY+REVIEW | Search PRIORITY+REVIEW |
| 7 | CENTRALISED PROCEDURE | 2 | 67% | 0% | 2 | Search CENTRALISED+PROCEDURE | Search CENTRALISED+PROCEDURE |
| 8 | FOOD AND DRUG ADMINISTRATION APPROVAL | 2 | 67% | 0% | 2 | Search FOOD+AND+DRUG+ADMINISTRATION+APPROVAL | Search FOOD+AND+DRUG+ADMINISTRATION+APPROVAL |
| 9 | ICH E5 GUIDELINE | 2 | 67% | 0% | 2 | Search ICH+E5+GUIDELINE | Search ICH+E5+GUIDELINE |
| 10 | REGISTRATION TRIAL | 2 | 67% | 0% | 2 | Search REGISTRATION+TRIAL | Search REGISTRATION+TRIAL |
Key Words Plus |
| Rank | Web of Science journal category | Relevance score (tfidf) |
Class's shr. of term's tot. occurrences |
Shr. of publ. in class containing term |
Num. of publ. in class |
|---|---|---|---|---|---|
| 1 | DRUG LAG | 6 | 80% | 1% | 4 |
| 2 | APPROVALS | 6 | 50% | 2% | 8 |
| 3 | DEVICES EVALUATION CENTER | 6 | 100% | 1% | 4 |
| 4 | ADMINISTRATION MODERNIZATION ACT | 4 | 75% | 1% | 3 |
| 5 | USER FEE ACT | 4 | 75% | 1% | 3 |
| 6 | ICH E5 GUIDELINE | 3 | 100% | 1% | 3 |
| 7 | PMDEC | 3 | 100% | 1% | 3 |
| 8 | MULTI REGIONAL TRIALS | 2 | 67% | 0% | 2 |
| 9 | UNDERSTANDING COMPARISONS | 2 | 67% | 0% | 2 |
| 10 | DISCONTINUATIONS | 1 | 38% | 1% | 3 |
Journals |
Reviews |
| Title | Publ. year | Cit. | Active references |
% act. ref. to same field |
|---|---|---|---|---|
| Trends in development and approval times for new therapeutics in the United States | 2003 | 98 | 9 | 100% |
| Evaluation of Oncology Drugs at the European Medicines Agency and US Food and Drug Administration: When Differences Have an Impact on Clinical Practice | 2011 | 21 | 2 | 100% |
| Industry funding of the FDA: Effects of PDUFA on approval times and withdrawal rates | 2005 | 36 | 7 | 71% |
| Racial/Ethnic Differences in Drug Disposition and Response: Review of Recently Approved Drugs | 2015 | 3 | 32 | 25% |
| Drug-review deadlines and safety problems | 2008 | 57 | 5 | 40% |
| European Union Centralised Procedure for marketing authorisation of oncology drugs: An in-depth review of its efficiency | 2006 | 7 | 2 | 100% |
| Approval probabilities and regulatory review patterns for anticancer drugs in the European Union | 2013 | 4 | 22 | 32% |
| FDA Review Divisions: Performance Levels and the Impact on Drug Sponsors | 2012 | 3 | 3 | 67% |
| Clinical trials for registration in the European Union: the EMEA 5-year experience in oncology | 2002 | 11 | 2 | 100% |
| Critical review of 'Public domain application': a flexible drug approval system in Japan | 2013 | 3 | 3 | 33% |
Address terms |
| Rank | Address term | Relevance score (tfidf) |
Class's shr. of term's tot. occurrences |
Shr. of publ. in class containing term |
Num. of publ. in class |
|---|---|---|---|---|---|
| 1 | OFF PHARMACEUT IND | 9 | 83% | 1.0% | 5 |
| 2 | STUDY DRUG DEV | 4 | 31% | 2.3% | 11 |
| 3 | PHARMACEUT REGULATORY SCI | 4 | 38% | 1.7% | 8 |
| 4 | CLIN TRIAL GUIDANCE | 3 | 100% | 0.6% | 3 |
| 5 | REVIEW AUDIT | 3 | 100% | 0.6% | 3 |
| 6 | TUFTS STUDY DRUG DEV | 2 | 17% | 1.9% | 9 |
| 7 | PHARMACEUT MED DEVICES EVALUAT | 1 | 21% | 1.2% | 6 |
| 8 | SOCIOL SUBJECT GRP | 1 | 33% | 0.4% | 2 |
| 9 | YOUNG LEADERS PROGRAM HLTH CARE ADM | 1 | 33% | 0.4% | 2 |
| 10 | CONSUMER LIAISON GRP | 1 | 50% | 0.2% | 1 |
Related classes at same level (level 1) |
| Rank | Relatedness score | Related classes |
|---|---|---|
| 1 | 0.0000197424 | ORPHAN DRUGS//RARE DISEASES//OFF ORPHAN PROD DEV |
| 2 | 0.0000180479 | MULTIPLE INDUSTRIES//RETURN ON INNOVATION//VALUE TRANSFERENCE |
| 3 | 0.0000159126 | PHARMACEUTICALISATION//CRHAM//CORPORATE BIAS |
| 4 | 0.0000158644 | FOOD AND DRUG LAW JOURNAL//HUMANITARIAN DEVICE EXEMPTION//PREMARKET APPROVAL |
| 5 | 0.0000130990 | GENERIC SUBSTITUTION//GENERIC DRUGS//REFERENCE PRICING |
| 6 | 0.0000111825 | CLINICAL TRIAL RISK//CONTINUOUS IMPROVEMENT//STRATEGIE IND |
| 7 | 0.0000085392 | HEALTH INSURANCE CLAIMS//MED HOSP MED CARE ADM//HEALTH INSURANCE CLAIM |
| 8 | 0.0000066612 | DRUG SHORTAGES//VACCINE STOCKPILES//VACCINE SHORTAGE |
| 9 | 0.0000062921 | BRIDGING STUDY//MULTIREGIONAL CLINICAL TRIAL//MULTIREGIONAL TRIAL |
| 10 | 0.0000061353 | ACTIVATION SYNDROME//RISK EVALUATION AND MITIGATION STRATEGIES//REGULATORY ACTIONS |