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Page | Keyword count |
TITLE I: GENERAL ISSUES | |
CHAPTER 2: Definitions and general provision | |
Article 3: Definitions | 3 |
TITLE II: REGISTRATION OF SUBSTANCES | |
CHAPTER 1: General obligation to register and information requirements | |
Article 9: Exemption from the general obligation to register for product and process orientated research and development (PPORD) | 3 |
CHAPTER 2: Substances regarded as being registered | |
Article 15: Substances in plant protection and biocidal products | 2 |
CHAPTER 4: Common provisions for all registrations | 1 |
Article 21: Manufacturing and import of substances | 11 |
Article 22: Further duties of registrants | 1 |
TITLE III: DATA SHARING AND AVOIDANCE OF UNNECESSARY TESTING | |
CHAPTER 1: Objectives and general rules | |
Article 25: Objectives and general rules | 1 |
CHAPTER 3: Rules for phase-in-substances | |
Article 28: Duty to pre-register for phase-in substances | 2 |
TITLE VI: EVALUATION | |
CHAPTER 4: Common provisions | |
Article 50: Registrants' and downstream users' rights | 6 |
TITLE XII: INFORMATION | |
Article 120: Cooperation with third countries and international organisations | 1 |
TITLE XV: TRANSITIONAL AND FINAL PROVISIONS | |
Article 128: Free movement | 1 |
ANNEX I: GENERAL PROVISIONS FOR ASSESSING SUBSTANCES AND PREPARING CHEMICAL SAFETY REPORTS | |
0.: INTRODUCTION | 2 |
ANNEX II: REQUIREMENTS FOR THE COMPILATION OF SAFETY DATA SHEETS | |
15.: SECTION 15: Regulatory information | 1 |
Appendix 11 | 1 |