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L1 Series Overview of Ethereum 2.0

TL;DR; Ethereum 2.0 is a new PoS chain that introduces sharding and eWASM as new features (=scalability & performance). ETH1 will be migrated to ETH2, at which point the long-planned transition from PoW to PoS will be complete.

L1 Series  Overview of Ethereum 2.0 1

The roadmap for updating to the new chain is divided into three phases, each of which presents an upgrade compared to the current chain: Phase 0 Beacon Chain (PoS), Phase 1 Sharding Phase 2 eWASMWhy PoS?PoS replaces the need run specialized hardware (& spend electricity) to validate txs. In PoW, dishonest actors lose tx fees.

In PoS, they lose tx fees & stake. PoS is also a prerequisite for sharding. The migration has been planned since the early days of EthereumPhase 0 Beacon ChainIs the new PoS chain to which all the shards connect to.

ETH1 tokenholders can move their tokens to the Beacon Chain and start validating (required stake: 32 ETH). For early validators on the new chain, the suggested inflation rewards are substantial. Why Sharding?

Sharding increases tx throughput with parallel processing. Data is stored and transactions executed on a specific shard by a smaller group of validators, instead of each validator storing the entire state and processing all transactions.Phase 1 ShardingEthereum 2.

L1 Series  Overview of Ethereum 2.0 2

0 will introduce 64 individual shard chains (recently downgraded from 1,024) with the option to add more. Periodically, the current state of each shard is recorded in a Beacon Chain block. Shard validators attest to the shards contents & state.

Why eWASM?Wasm is a new fast, efficient and portable format standard for executable programs. eWASM is a subset used for Ethereum contracts.

eWASM uses hardware capabilities to execute programs faster. Developers can use familiar languages (eg. Rust/C) and tools & libraries.

Phase 2 eWASMeWASM replaces Ethereums current virtual machine (EVM). Existing Solidity contracts will be compatible with eWASM. Only once eWASM is launched, smart contracts will be able to execute on ETH2.

Beyond Phase 2Improved support in the VM for STARKs to further improve scalability and privacy. Because cross-shard transactions are asynchronous (slow), further work on transacting between shards will need to be done (such as L2 solutions that work across shards).In short, only after phase 2 will Ethereum 2.

0 be fully functional. Phase 0, only staking will be enabled (Q2 2020). Phase 1, data can be stored on shards but no txns executed (Q1 2021).

Phase 2, smart contracts can be executed (2022). Deprecating ETH1There will be two different ether tokens during the transition. The original plan was to roll the PoW state into one of the shards.

According to a new plan ETH1 is transferred to its own shard but now without PoW (miners replaced with ETH2 validators). Validation on ETH2The only requirement for validating is to stake 32 ETH. Anyone can join, and a minimum of 100 validators are randomly selected to produce blocks.

This is different from e.g. Polkadot, where validators are nominated by token holders.

GovernanceEthereum 2. 0 continues with off-chain governance. Why?

In Vitaliks view, explicit governance design is difficult and a bad implementation creates unexpected issues. On-chain governance also has practical problems like low voter turnout. Terminal provides financial and business metrics on crypto protocols metrics were used to seeing applied to traditional companies, e.

g the P/E ratio. Crypto protocols operate like traditional businesses, only they do it directly on the Internet.For more, check out Token Terminals website and Twitter RELATED QUESTION What are the reporting timelines for adverse event arising from medical devices?

I have been in the hospital management, consulting and now recently in the medical devices area for close to two decades in India. This answer is related to AEs in hospitals and particularly in the context of NABH requirements in India. The reporting timelines for adverse events (AEs) is irrespective of the source - arising from medical devices, drugs and consumables, processes or people.

Everywhere across the globe the expected timeline depends mainly on factors such as - Severity (e.g. whether caused death, is life-threatening, potentially life-threatening or not), but also on itsNature - Expected/ UnexpectedCausality - Definitely / Probably / Possibly related to u2026Depending on the severity and nature of the AE the timelines expected for reporting could vary from within 24 hours to 30 days.

High severity cases in a hospital setting is much rarer than in case of Clinical research or studies. NABH does not really strictly define specific timelines for hospitals to report. However they expect a process and timeline to be defined internally, reporting mechanism to be in place and data is expected to be analysed by specific Care committees on periodic basis and corrective / preventive actions to be put in place.

Most hospitals follow incident reporting practice and usually furnish collated reports to Patient Care committee on a monthly or quarterly basis. In order to ensure patient and care-giver safety and prevention of AEs due to medical equipment, NABH requires hospitals to carry outQA (Quality Assurance) and Calibration of medical equipment on periodic basis,adhere to AERB regulations in case of radiation equipmentcarry out periodic preventive maintenanceConduct user training for proper usage and handling of medical equipmentTraining for handling hazardous materialsafe and responsible disposal of condemned equipmentand also encourages following incident reporting/ corrective actionWhat are the reporting timelines for adverse event arising from medical devices?

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